Cdrh Regulations - Utax CLP 3721 Instruction Manual

CDRH Regulations

The Center for Devices and Radiological Health (CDRH) of the U.S. Food
and Drug Administration implemented regulations for laser products on
August 2, 1976. These regulations apply to laser products manufactured
after August 1, 1976. Compliance is mandatory for products marketed in
the United States. A label indicating compliance with the CDRH
regulations must be attached to laser products marketed in the United
States.
Canadian Department of Communications Compliance
Statement
This Class B digital apparatus complies with Canadian ICES-003.
Avis de conformité aux normes du ministère des
Communications du Canada
Cet appareil numérique de la classe B est conforme à la norme NMB-003
du Canada.
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