Safety and Regulatory
CDRH regulations (USA only)
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 from August 1,
1976. Compliance is mandatory for products marketed in the United States. The labels and artwork shown below indicate compliance with CDRH regulations and must be attached to laser products marketed in the United States.
WARNING: Use of controls or adjustments, or performing procedures other than those specified in this manual may result in hazardous laser radiation exposure.
Note: Complies with 21 CFR Chapter 1 Subchapter J.
Laser Class Information: A black on yellow label which reads, “Class 1 Laser Product” printed in English, French, German, Finnish, Japanese, and Spanish.
Compliance with International Regulations
All HP systems equipped with laser devices comply with appropriate safety standards, including IEC825.