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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 K062602
Device Name BAND-AID(R) BRAND LIQUID BANDAGE
Applicant
JOHNSON & JOHNSON CONSUMER COMPANIES, INC.
199 GRANDVIEW ROAD
SKILLMAN,  NJ  08558 -9498
Applicant Contact MICHELLE R TURK
Correspondent
JOHNSON & JOHNSON CONSUMER COMPANIES, INC.
199 GRANDVIEW ROAD
SKILLMAN,  NJ  08558 -9498
Correspondent Contact MICHELLE R TURK
Regulation Number880.5090
Classification Product Code
KMF  
Date Received09/01/2006
Decision Date 12/11/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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