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GUIDANCE DOCUMENT

Optional Interlocks - Labeling (Laser Notice 17) March 1977

Final
Issued by:
Guidance Issuing Office
Center for Devices and Radiological Health

Food and Drug Administration notice to all manufacturers and potential manufacturers of Laser Products regarding optional interlocks and related labeling, 21 CFR 1O4O.lO(f)(2) and (g).


Submit Comments

Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All comments should be identified with the title of the guidance.