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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 K930174
Device Name GLASSES MOLASSES
Applicant
ARTHUR F. KOZAKOWSKI, JR.
RD #1 BOX 221
HERKIMER,  NY  13350
Applicant Contact ARTHUR F KOZAKOWSKI
Correspondent
ARTHUR F. KOZAKOWSKI, JR.
RD #1 BOX 221
HERKIMER,  NY  13350
Correspondent Contact ARTHUR F KOZAKOWSKI
Regulation Number886.5842
Classification Product Code
HQZ  
Date Received01/13/1993
Decision Date 01/25/1994
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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