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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name spectacle, magnifying
510(k) Number K813548
Device Name UVEX MINI-SPECS
Applicant
BACOU USA, INC. AND UVEX SAFETY, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BACOU USA, INC. AND UVEX SAFETY, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number886.5840
Classification Product Code
HOI  
Date Received12/21/1981
Decision Date 03/02/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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