Agency Notices

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 from August 1, 1976. Compliance is mandatory for products marketed in the United States.

Compliance with International Regulations

All systems equipped with CD-ROM drives comply with appropriate safety standards including IEC 825.

Laser Product Label

The following label or equivalent is located on the surface of laser products:

This label indicates that the product is classified as a CLASS 1 LASER PRODUCT. This label appears on a laser device installed in the product.

If you have an LS-120 drive or an LS-260 drive, this label is located next to the Class 1 Laser Product label on the system.

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Safety & Regulatory Information