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GUIDANCE DOCUMENT

Lasers Manufactured and Used In-House (Laser Notice 14) November 1976

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

TO: All Manufacturers and Potential Manufactures of Laser Products

SUBJECT: Applicability of the Performance Standard to Products Manufactured by a Company For Use in its Manufacturing Process


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.