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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name electrode, corneal
510(k) Number K926540
Device Name SOPHER AND BIERER OVUM FORCEPS
Applicant
THOMASVILLE MEDICAL ASSOC.
935 COBBLESTONE COURT
ALPHARETTA,  GA  30201
Applicant Contact THOMAS J ZINNANTI
Correspondent
THOMASVILLE MEDICAL ASSOC.
935 COBBLESTONE COURT
ALPHARETTA,  GA  30201
Correspondent Contact THOMAS J ZINNANTI
Regulation Number886.1220
Classification Product Code
HLZ  
Date Received12/30/1992
Decision Date 02/25/1994
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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