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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stand, Instrument, Ac-Powered, Ophthalmic
510(k) Number K832073
Device Name ELECTRIC INSTRUMENT TABLE
Applicant
COOPERVISION, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
COOPERVISION, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number886.1860
Classification Product Code
HMF  
Date Received06/28/1983
Decision Date 08/12/1983
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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