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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Frame, Spectacle
510(k) Number K931135
Device Name ALTAIR EYEWEAR FRAMES
Applicant
Altair Eyewear
10419 Old Pl.rville Rd.
Suite 270
Sacramento,  CA  95825
Applicant Contact STEVE WRIGHT
Correspondent
Altair Eyewear
10419 Old Pl.rville Rd.
Suite 270
Sacramento,  CA  95825
Correspondent Contact STEVE WRIGHT
Regulation Number886.5842
Classification Product Code
HQZ  
Date Received03/05/1993
Decision Date 08/02/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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