C
C
S
R
I
AFETY AND
EGULATORY
NFORMATION
CDRH R
(USA O
)
EGULATIONS
NLY
The Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug Administration implemented reg-
ulations for laser products on August 2, 1976. These regulations apply to laser products manufactured from August 1,
1976. Compliance is mandatory for products marketed in the United States. The labels and artwork shown below indi-
cate compliance with CDRH regulations and must be attached to laser products marketed in the United States.
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WARNING:Use of controls, adjustments or performing procedures other than those specified in this manual may result in haz-
ardous laser radiation exposure.
NOTE:
Complies with 21 CFR Chapter 1 Subchapter J.
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Laser Class Information: A black on yellow label which reads, "Class 1 Laser Product" printed in English, French, Ger-
man, Finnish, Japanese, and Spanish.
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CONTENTS
INDEX
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