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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Forceps, General & Plastic Surgery
510(k) Number K853153
Device Name MEDUS GMBH
Applicant
Corkes Medical Co.
1371 9th Ave.
Suite 2
San Francisco,  CA  94122
Applicant Contact PIERRE KESRAWANI
Correspondent
Corkes Medical Co.
1371 9th Ave.
Suite 2
San Francisco,  CA  94122
Correspondent Contact PIERRE KESRAWANI
Regulation Number878.4800
Classification Product Code
GEN  
Date Received07/29/1985
Decision Date 08/07/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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