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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name bandage, liquid
510(k) Number K936052
Device Name BRADY MEDICAL PRODUCTS HYSORB(TM) WOUND DRESSING
Applicant
BRADY MEDICAL PRODUCTS CO.
727 W. GLENDALE AVE.
P.O. BOX 571
MILWAUKEE,  WI  53201
Applicant Contact WALLACE K REAMS
Correspondent
BRADY MEDICAL PRODUCTS CO.
727 W. GLENDALE AVE.
P.O. BOX 571
MILWAUKEE,  WI  53201
Correspondent Contact WALLACE K REAMS
Regulation Number880.5090
Classification Product Code
KMF  
Date Received12/20/1993
Decision Date 03/07/1994
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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