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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 K932913
Device Name FERRIS POLYMEM HYDROPHILIC WOUND DRESSING
Applicant
FERRIS MFG. CORP.
16W300 83RD ST.
BURR RIDGE,  IL  60527 -5848
Applicant Contact JEFFREY A DZIURA
Correspondent
FERRIS MFG. CORP.
16W300 83RD ST.
BURR RIDGE,  IL  60527 -5848
Correspondent Contact JEFFREY A DZIURA
Regulation Number880.5090
Classification Product Code
KMF  
Date Received06/16/1993
Decision Date 06/07/1994
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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