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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Drape, Surgical, Antimicrobial
510(k) Number K880513
Device Name DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE
Applicant
Taub Industries
465 W. Broadway
New York,  NY  10012
Applicant Contact TAUB, M.D.
Correspondent
Taub Industries
465 W. Broadway
New York,  NY  10012
Correspondent Contact TAUB, M.D.
Regulation Number878.4370
Classification Product Code
KKX  
Date Received02/09/1988
Decision Date 03/11/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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