Title: Test Protocol for Comparative Evaluation of Protective Gloves for
Law Enforcement and Corrections Applications
Series: N/A
Author: NIJ
Published: June 1999
Subject: police equipment
pages: 15
bytes: 28kb

Figures, charts, forms, and tables are not included in this ASCII plain-text
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graphic file available from this Web site or order a print copy from
NLECTC at 800-248-2742.

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U.S. Department of Justice
Office of Justice Programs 
National Institute of Justice

National Institute of Justice
Law Enforcement and Corrections Standards and Testing Program

Test Protocol for Comparative Evaluation of Protective Gloves for Law
Enforcement and Corrections Applications
NIJ Test Protocol 99-114

-------------------------------

ABOUT THE LAW ENFORCEMENT AND CORRECTIONS 
STANDARDS AND TESTING PROGRAM

The Law Enforcement and Corrections Standards and Testing Program is
sponsored by the Office of Science and Technology of the National
Institute of Justice (NIJ), U.S. Department of Justice. The program
responds to the mandate of the Justice System Improvement Act of 1979,
which created NIJ and directed it to encourage research and development
to improve the criminal justice system and to disseminate the results to
Federal, State, and local agencies.

The Law Enforcement and Corrections Standards and Testing Program is
an applied research effort that determines the technological needs of
justice system agencies, sets minimum performance standards for specific
devices, tests commercially available equipment against those standards,
and disseminates the standards and the test results to criminal justice
agencies nationally and internationally.

The program operates through:

The Law Enforcement and Corrections Technology Advisory Council
(LECTAC) consisting of nationally recognized criminal justice
practitioners from Federal, State, and local agencies, which assesses
technological needs and sets priorities for research programs and items to
be evaluated and tested.

The Office of Law Enforcement Standards (OLES) at the National
Institute of Standards and Technology, which develops voluntary national
performance standards for compliance testing to ensure that individual
items of equipment are suitable for use by criminal justice agencies. The
standards are based upon laboratory testing and evaluation of
representative samples of each item of equipment to determine the key
attributes, develop test methods, and establish minimum performance
requirements for each essential attribute. In addition to the highly
technical standards, OLES also produces user guides that explain in
nontechnical terms the capabilities of available equipment.

The National Law Enforcement and Corrections Technology Center
(NLECTC), operated by a grantee, which supervises a national
compliance testing program conducted by independent laboratories. The
standards developed by OLES serve as performance benchmarks against
which commercial equipment is measured. The facilities, personnel, and
testing capabilities of the independent laboratories are evaluated by OLES
prior to testing each item of equipment, and OLES helps the NLECTC
staff review and analyze data. Test results are published in Equipment
Performance Reports designed to help justice system procurement
officials make informed purchasing decisions.

Publications are available at no charge from the National Law
Enforcement and Corrections Technology Center. Some documents are
also available online through the Internet/World Wide Web. To request a
document or additional information, call 800-248-2742 or 301-519-5060,
or write:

National Law Enforcement and Corrections Technology Center
P.O. Box 1160
Rockville, MD 20849-1160
E-Mail: asknlectc@nlectc.org
World Wide Web address: http:www.nlectc.org



The National Institute of Justice is a component of the Office of Justice
Programs, which also includes the Bureau of Justice Assistance, Bureau of
Justice Statistics, Office of Juvenile Justice and Delinquency Prevention,
and the Office for Victims of Crime.

-------------------------------

U.S. Department of Justice
Office of Justice Programs
National Institute of Justice

Test Protocol for Comparative Evaluation of Protective Gloves for Law
Enforcement and Corrections Applications

NIJ Test Protocol 99-114

Alim A. Fatah
National Institute of Standards and Technology
Office of Law Enforcement Standards
Gaithersburg, MD 20899-8102

Prepared for:
National Institute of Justice
Office of Science and Technology
U.S. Department of Justice
Washington, DC 20531

June 1999

-------------------------------

National Institute of Justice
Jeremy Travis
Director

The technical effort to develop this test protocol was conducted under
Interagency Agreement 94-IJ-R-004, Project No. 97-009 IA/CTT.

This test protocol was formulated by the Office of Law Enforcement
Standards (OLES) of the National Institute of Standards and Technology
(NIST) under the direction of Alim A. Fatah, Program Manager,
Chemical Systems and Materials, and Kathleen M. Higgins, Director of
OLES. The preparation of this test protocol was sponsored by the

National Institute of Justice, David G. Boyd, Director, Office of Science
and Technology.

This test protocol has been reviewed and approved by the Weapons and
Protective Systems Subcommittee and the Executive Committee of the
Law Enforcement and Corrections Technology Advisory Council.

-------------------------------

FOREWORD

This document, NIJ Test Protocol 99-114: Test Protocol for Comparative
Evaluation of Protective Gloves for Law Enforcement and Corrections
Applications, is a comparative evaluation protocol developed by the
Office of Law Enforcement Standards of the National Institute of
Standards and Technology. It is produced as part of the Law Enforcement
and Corrections Standards and Testing Program of the National Institute
of Justice. A brief description of the program appears on the inside front
cover.

This test protocol is a technical document that evaluates performance and
other requirements that equipment should meet to satisfy the needs of
criminal justice agencies for high-quality service. Purchasers can use the
test methods described in this test protocol to evaluate whether a particular
piece of equipment meets the agency's essential requirements, or they may
have the tests conducted on their behalf by a qualified testing laboratory.
NIJ, through its National Law Enforcement and Corrections Technology
Center (NLECTC)- National, conducts periodic comparative evaluations
of products in accordance with the test methods outlined in this protocol
and publishes the data. These reports can be utilized by agencies to assist
in selecting products that best meet their requirements. For copies of the
most recent evaluations conducted, contact NLECTC at 800-248-2742 or
301-519-5060. 

Because this NIJ test protocol is designed as a procurement aid, it
provides precise and detailed test methods. For those who seek general
guidance concerning the selection and application of law enforcement
equipment, user guides have also been published. The guides explain in
nontechnical language how to select equipment capable of the
performance required by an agency.

NIJ test protocols are subjected to continuing review. Technical comments
and recommended revisions are welcome. Please send suggestions to the
Director, Office of Science and Technology, National Institute of Justice,
U.S. Department of Justice, 810 7th St., NW, Washington, DC 20531.



Before citing this or any other NIJ test protocol in a contract document,
users should verify that the most recent edition of the test protocol is used.
Write to: Director, Office of Law Enforcement Standards, National
Institute of Standards and Technology, 100 Bureau Drive, Stop 8102,
Gaithersburg, MD 20899-8102.

David G. Boyd, Director
Office of Science and Technology
National Institute of Justice

NIJ TEST PROTOCOL FOR COMPARATIVE EVALUATION OF
PROTECTIVE GLOVES FOR LAW ENFORCEMENT AND
CORRECTIONS APPLICATIONS

CONTENTS
Foreword
1.--Purpose and Scope
2.--Applicable Documents
3.--Requirements
--3.1--Description
--3.2--Rating Types
4.--Test Methods
--4.1--Pathogenic Resistance
--4.2--Dexterity
--4.3--Cut Resistance
--4.4--Tear Resistance
--4.5--Puncture Resistance
5.--Quality Assurance
--5.1--Responsibility for Inspection
--5.2--Manufacturer Quality Assurance Plan
--5.3--Examination Procedure
--5.4--Test Procedures
--5.5--Reporting the Test Results
6.--Workmanship, Labeling, and Acceptance Requirements for Protective
Gloves
--6.1--Acceptance Criteria
--6.2--Test Sequence
--6.3--Workmanship
--6.4--Labeling
7.--Certification of Testing in Accordance with NIJ Test Protocols




Commonly Used Symbols and Abbreviations

A--ampere------H--henry----nm--nanometer
ac--alternating current--h--hr--hour----No.--number
AM--amplitude modulation--hf--high frequency--o.d.--outside diameter
cd--candela--Hz--hertz (c/s)
cm--centimeter----i.d.--inside diameter--p.--page
CP--chemically pure----in--inch*------Pa--pascal
c/s--cycle per second*--ir--infrared----pe--probable error
d--day--J--joule--pp.--pages
dB--decibel--L--lambert--ppm--part per million
dc--direct current--L--liter--qt--quart*
(C--degree Celsius----lb--pound*--rad--radian
(F--degree Fahrenheit*--lbf--pound-force*--rf--radio frequency
diam--diameter--lbf(in--pound-force inch*--rh--relative humidity
emf--electromotive force--lm--lumen--s--second
eq--equation--ln--logarithm (natural)--SD--standard deviation
F--farad--log--logarithm (common)--sec.--section
fc--footcandle*--M--molar--SWR--standing wave ratio
fig.--figure--m--meter--uhf--ultrahigh frequency
FM--frequency modulation--min--minute--uv--ultraviolet
ft--foot*--mm--millimeter--V--volt
ft/s--foot per second*--mph--mile per hour*--vhf--very high frequency
g--acceleration--m/s--meter per second--W--watt
g--gram--N--newton
gr--grain*--wt--weight

COMMON CONVERSIONS
(See ASTM E380)

ft/s ( 0.3048000=m/s--------lb x 0.4535924=kg
ft ( 0.3048=m----------lbf x 4.448222=N
ft(lbf ( 1.355818=J----------lbf/ft x 14.59390=N/m
gr ( 0.06479891=g--------lbf in x 0.1129848=N(m
in ( 2.54=cm----------lbf/in2 x 6894.757=Pa
kWh (3600000=J----------mph x 1.609344=km/h
qt x 0.9463529=L

Temperature: (T degrees F-32)x5/9=T degrees C
Temperature: (T degrees Cx9/5)+32=T degrees F

*These units are not in the metric system of units, but are included for the
convenience of the user.



NIJ TEST PROTOCOL FOR COMPARATIVE EVALUATION OF
PROTECTIVE GLOVES FOR LAW ENFORCEMENT AND
CORRECTIONS APPLICATIONS

1. PURPOSE AND SCOPE 

The purpose of this test protocol is to compare the performance of
protective gloves for use by law enforcement, corrections, and military
personnel. The scope of this test protocol is limited to the types of gloves
that meet the rating levels described in Section 3.2 of this test protocol.
The applicable documents, which are in Section 2.0, describe the test
methods for conducting the comparative evaluation of the protective
gloves and are incorporated as part of this test protocol.

2. APPLICABLE DOCUMENTS

2.1--Government Documents 
The most current versions of the following referenced documents should
be used.

Federal
Code of Federal Regulations (CFR)[1]

a. 29 CFR 1910 Part 1030--"Occupational Exposure to Bloodborne
Pathogens: Final Rule," Federal Register, Vol. 56, No. 235, Dec. 6, 1991,
pp. 64175-64182 (Occupational Safety and Health Administration).

b. 16 CFR Part 1500.3--Definitions of Toxic and Hazardous Materials.

c. 16 CFR 423, Part 423 --Care Labeling of Textile Wearing Apparel and
Certain Piece Goods, as amended effective January 2, 1984; Federal Trade
Commission Regulation Rule.

2.2--Non-Government Documents 
The most current versions of the following referenced standards should be
used.

2.2.1--American National Standards Institute (ANSI)/American Society
for Quality Control (ASQC)[2]
ANSI/ASQC Z1.4--Sampling Procedures and Tables for Inspection by
Attributes.

2.2.2--National Fire Protection Association (NFPA)[3]
NFPA 1999--Standard on Protective Clothing for Emergency Medical
Operations.

2.2.3--American Society for Testing and Materials (ASTM)[4]
ASTM D 5151--Standard Test Method for Detection of Holes in Medical
Gloves.

ASTM F 1671--Standard Test Method for Resistance of Materials Used in
Protective Clothing to Penetration by Blood-Borne Pathogens Using
Phi-X174 Bacteriophage Penetration as a Test System.

ASTM F 1342--Standard Test Method for Protective Clothing Material
Resistance to Puncture.

ASTM F 1790--Standard Test Method for Measuring Cut Resistance of
Materials Used in Protective Clothing.

ASTM D 5712--Standard Test Method for Analysis of Protein in Natural
Rubber and its Products.

ASTM D 2582--Standard Test Method for Puncture-Propagation Tear
Resistance of Plastic Film and Thin Sheeting.

2.2.4 British/European Standards[5]
BS EN 420:1994--General Requirements for Gloves.
BS EN 388:1994--Protective Gloves Against Mechanical Risks.

Table 1.--Protective Glove Rating Matrix
Type---A-Pathogenic Resistant (Biohazard); B-Cut Resistant (Blade); C-
Puncture Resistant (Needle)
Criteria
Pathogenic--Pass--Pass/Fail/NT--Pass/Fail/NT
Dexterity--High/Moderate--Low/Moderate--Low/Moderate
Tear--High/Moderate--High/Moderate--High/Moderate
Cut--Rating/NT--High--High/Moderate/NT
Puncture--Rating/NT--High/Moderate/NT--High

Notes for Table 1 Ratings:

a) Cut Resistance
--Low = Less than 5 N (<1.124 lbf)
--Moderate = 6 N to 15 N (1.349 lbf to 3.372 lbf)
--High = 16 N to 40 N (3.60 lbf to 8.99 lbf) or higher

b) Puncture Resistance
--Low = 20 N to 59 N (4.496 lbf to 13.264 lbf)
--Moderate--= 60 N to 99 N (13.489 lbf to 22.257 lbf)
--High = 100 N to 150 N (22.482 lbf to 33.723 lbf) or higher

c) Tear Resistance
--Low = 10 N to 24 N (2.248 lbf to 5.396 lbf)
--Moderate = 25 N to 49 N (5.621 lbf to 11.016 lbf)
--High = 50 N to 75 N (11.241 lbf to 16.862 lbf) or higher

d) Dexterity
--Poor = can pick up only 11 mm diameter pins
--Low = can pick up only 9.5 mm diameter pins
--Moderate = can pick up 6.5 mm diameter pins
--High = can pick up 5 mm diameter pins

e) NT--Not tested (Gloves that are not claimed by the manufacturer as a
given type of glove need not be tested against that Type Criteria, e.g., a
cut resistant glove which is not claimed to be puncture resistant need not
undergo a puncture test).

3. REQUIREMENTS

3.1--Description 
The protective gloves covered by this test protocol are required to meet
the performance criteria and rating types defined for each criterion in
accordance with Table 1.

3.2--Rating Types 
There are three major rating types designated as Types A, B, and C. If
technically and commercially feasible, a glove that combines all the
performance requirements of types A, B, and C, is rated the highest.

3.2.1--Type A 
This glove shall be specifically designed for protection against biological
hazards. It shall provide general protection against health hazards in
dealing with field interrogation, apprehension, transport, and incarceration
of suspects and/or prisoners as well as crime scene investigation and
evidence gathering.


3.2.2--Type B 
This glove is specifically designed to be cut resistant. It shall provide
general protection against health hazards in dealing with field
interrogation, apprehension, and incarceration of suspects/prisoners as
well as crime scene investigation and evidence gathering in hostile
environments where sharp objects such as knives and razor blades may
pose a threat.

3.2.3--Type C 
This glove is specifically designed to be puncture resistant. It shall
provide general protection against health hazards in dealing with field
interrogation, apprehension, and incarceration of suspects/prisoners as
well as crime scene investigation and evidence gathering in hostile
environments where pointed and needle shaped objects may pose a threat.
These gloves are intended for use while frisking or patting down suspects/
prisoners.

4. TEST METHODS

The performance criteria that the protective gloves in this test protocol are
evaluated against are defined as follows:

4.1--Pathogenic Resistance 
Pathogenic resistance gloves shall provide protection against common
blood-borne infectious diseases. The gloves meeting this criterion shall
provide protection against microbiological pathogens that are transmitted
through physical contact or contact with bodily fluids, such as blood,
saliva, semen, etc. The gloves shall form a barrier to both the pathogen
and/or the carrier fluid when tested in accordance with NFPA 1999,
Sections 6-9 and 6-10, and the ASTM Standards cited therein. The test
method measures the resistance of a protective material to penetration by
blood-borne pathogen and for leakage, using a surrogate microbe under
conditions of continuous liquid contact. Protective clothing material
pass/fail determination is based on the detection of viral penetration
and/or glove leakage.

4.2--Dexterity 
The gloves meeting this performance criterion shall meet the dexterity
requirements when tested in accordance with British European Standard
BS EN 420:1994, Section 5.2. In this test, a subject wearing the test glove
is instructed to pick a series of pins of similar length but differing
diameters. The dexterity is rated according to the smallest pin diameter
that the subject wearing the glove can pick up.

4.3--Cut Resistance 
The glove meeting this performance criterion shall provide protection
against slashes and/or cuts by sharp objects, such as blades and knives
when tested in accordance with ASTM F 1790. This test method is used to
measure the cut resistance of a material when mounted on a mandrel and
subjected to a cutting edge under a specified load.

4.4--Tear Resistance 
The glove meeting this performance criterion shall provide the tear
resistance when tested in accordance with British European Standard BS
EN 388:1994, Section 6.3. In this method a tensile tester is used to
measure the force necessary to tear a test specimen which is previously cut
in a defined manner. For gloves that are entirely made of elastomeric
materials such as plastic film, latex, etc., or have a liner made of such
materials, the recommended test for tear resistance of the elastomeric
material is ASTM D 2582. This test involves the determination of the
dynamic tear resistance of plastic film and thin sheeting subjected to
end-use snagging type hazards.

4.5--Puncture Resistance
The glove meeting this performance criterion shall be resistant to
penetration by needles and other pointed objects when tested in
accordance with ASTM F 1342. This test method determines the puncture
resistance of a protective clothing specimen by measuring the force
required to cause a sharp-edged puncture probe to penetrate through the
specimen.

5. QUALITY ASSURANCE PROVISIONS

5.1--Responsibility for Inspection
The manufacturer shall be responsible for the performance of all
inspection requirements as specified herein. Inspections and Quality
Assurance procedures shall comply with ANSI/ASQC Z1.4, Sampling
Procedures and Tables for Inspection by Attributes and OSHA Standard
29 CFR 1910.1030, Occupational Exposure to Blood-borne Pathogens:
Final Rule, Federal Register, Vol. 56, No 235, Dec. 6, 1991, pp.
64175-64182. Except as otherwise specified, the manufacturer may use
his/her own or any other facilities suitable for the performance of the
inspection requirements specified herein.

5.2--Manufacturer Quality Assurance Plan
The manufacturer shall develop and institute a quality assurance plan in
accordance with the standards listed in Section 4.l. This quality assurance
plan shall ensure that the product delivered meets the requirements
specified herein. Manufacturers should include a copy of this plan as part
of any model shipped to the purchaser.

5.3--Examination Procedure 
Lot numbers and results from the examination shall be recorded on the
inspection sheets for each box of gloves. The sample and/or its
components shall be examined for defects detailed in Section 6.3.

5.4--Test Procedures
Tests shall be performed in accordance with the following methods.
Reference to specific instruments is for information only; use of a
company and/or product name in this document does not imply approval
or recommendation of the product in preference to others that may also be
suitable. Test specimens for the cut (Sec. 4.3), tear (Sec. 4.4) and puncture
(Sec. 4.5) tests shall be cut from the finished glove in accordance with the
dimensions specified for each test method and from glove location(s)
specified in 

Figure 4, page 8 of BS EN Standard 388. Fourteen (14) pairs of gloves are
the minimum numbers of samples needed for each model submitted for
testing. Twelve (12) pairs will be used for testing and two (2) pairs will be
retained for archival purposes as indicated in Table 2 on page 7.

Table 2. Glove samples to be submitted for each model.

No.-----Test Method-----Minimum No. of Gloves to be Tested
1.--------Pathogenic--------------4 Pairs
2.--------Cut Resistance----------2 Pairs
3.--------Tear Resistance---------4 Pairs
4.--------Puncture Resistance----2 Pairs
5.--------Archive------------------2 Pairs

5.4.1--Pathogenic Resistance 
Tests for pathogenic resistance shall be as specified in Section 4.1.

5.4.2--Dexterity 
The dexterity requirements of the gloves in this test protocol shall be
tested as specified in Section 4.2

5.4.3--Cut Resistance
Tests for the cut resistance of the gloves shall be performed as specified in
Section 4.3.

5.4.4--Tear Resistance 
Tests for the tear resistance of the gloves shall be performed as specified
in Section 4.4.

5.4.5--Puncture Resistance 
Tests for the puncture resistance of the gloves shall be performed as
specified in Section 4.5.

5.5--Reporting the Test Results
The laboratory results shall be summarized in a table format listing each
glove model tested and how it performed against each of the performance
criteria listed in Sections 4.1 to 4.5 of this test protocol. Statistical
significance of the reported results as well as precision and accuracy of the
test measurement shall also be reported, wherever it is deemed applicable.

6. WORKMANSHIP, LABELING, AND ACCEPTANCE
REQUIREMENTS FOR PROTECTIVE GLOVES

6.1--Acceptance Criteria
A protective glove model satisfies the requirements of this test protocol if
all sample items meet the workmanship (see Sec. 6.3) and labeling (see
Sec. 6.4) requirements when tested in accordance with the performance
requirements of this test protocol. Each manufacturer must submit a
minimum of fourteen (14) pairs for each model for performance of the
tests required for this protocol. Any sample found not in compliance with
the workmanship and labeling requirements will be returned to the
manufacturer, at the manufacturer's expense, without further testing.

6.2--Test Sequence
Tests shall be conducted in the order presented in Sections 4.1 through 4.5
of this test protocol. In the event that one of the samples fails to meet any
requirement prior to the completion of testing, the laboratory shall
continue with the test sequence, if possible, to the full completion of the
performance requirements.

6.3--Workmanship
Each glove sample submitted shall be free from wrinkles, blisters, cracks,
or fabric tears; incomplete, inconsistent, or unsecured stitching; sharp or
rough edges or corners; and any other evidences of inferior workmanship.
The gloves shall not tear nor shall the stitching unravel during inspection
or while performing the tests specified in Sections 4.1 to 4.5. All samples
of a given model must be identical in appearance, materials of
construction, and manner of construction.

6.4--Labeling
Each set of protective gloves shall be clearly and durably marked (labeled)
in a readable type size, in the English (U.S.) language, in accordance with
the requirements set forth below. The label(s) must be securely attached to
each glove. For nonfabric (latex) gloves providing basic pathogen
protection, the manufacturer shall place the information required by this
section on the box or as an insert to accompany the gloves in their
intended packaging.

1.--Name, logo, or other identification of the manufacturer.

2.--The rated type of protection, according to Section 4.2 of this protocol
and referenced to the current edition of this test protocol.

3.--Size (if custom fitted, a provision for the name of the individual for
whom it is made).

4.--Lot number (a lot number is a control number assigned by the
manufacturer to the lot of material used to construct the gloves, and
should be used for traceability and quality control purposes).

5.--Line to write "Date of Issue."

6.--A model designation that uniquely identifies the glove for purchasing
purposes. For the purposes of this test protocol, a "model" is defined as a
manufacturer designation (name, number, or other description) that serves
to uniquely identify a specific protective glove configuration based upon
the details of the protective glove construction. Separate model
designations must be assigned to protective gloves which vary in materials
of construction (to include weave, denier, and waterproofing), manner of
construction (to include stitch patterns or other methods of assembling the
materials), and opening/closure configurations (i.e., hook and pile, zipper,
elastic).

7.--Care instructions for the gloves in accordance with 16 CFR 423, Part
423 Care Labeling of Textile Wearing Apparel and Certain Piece Goods,
as amended effective January 2, 1984; Federal Trade Commission
Regulation Rule [Not required for disposable or single-use gloves].

8.--A statement indicating that each glove model submitted for testing has
been tested for protein content in accordance with NFPA 1999, Section
6-15 and ASTM Test Method cited therein. This test method determines
the protein content of the glove material(s) and reports the average protein
content level in micrograms per gram of glove material(s).

7. CERTIFICATION OF TESTING IN ACCORDANCE WITH NIJ
TEST PROTOCOLS

Manufacturers are prohibited from placing any statement on the model of
protective glove (on the glove itself, the labeling, or accompanying
advertisement or documentation) that in any way states, infers, or
otherwise suggests that the model has been tested in accordance with the
NIJ TEST PROTOCOL FOR PROTECTIVE GLOVES, until such time
as the model has successfully completed testing at an NIJ-approved testing
facility for the purposes of this test protocol, and a letter has been issued
to the manufacturer by the National Law Enforcement and Corrections
Technology Center (NLECTC). At that time, the manufacturer may place
the following statement on the required labeling as specified in Section
6.4:

"The manufacturer certifies that this model of protective glove has been
tested in accordance with NIJ Test Protocol 99-114, dated June 1999."

Manufacturers, once authorized to use this statement, are prohibited from
modifying this statement in any fashion.

Footnotes:
[1]The CFR and Federal Register are for sale on a subscription basis by the
Superintendent of Documents, U.S. Government Printing Office (GPO),
Washington, DC 20402. Reprints of certain regulations may be obtained
from the Federal Agency responsible for their issuance.

[2]Copies may be obtained from the American National Standards Institute,
11 West 42nd Street, New York, NY 10036, Standardization Documents
Order Desk or from the American Society for Quality Control, 611 East
Wisconsin Avenue, Milwaukee, WI 53202.

[3]Copies may be obtained from the National Fire Protection Association, 1
Batterymarch Park, P.O. Box 9101, Quincy, MA 02269-9101.

[4]Copies may be obtained from the American Society for Testing and
Materials, 1916 Race Street, Philadelphia, PA 19103-1187.

[5]Copies may be obtained from the Document Center, 1504 Industrial
Way, Unit 9, Belmont, CA 94002-4044.