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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 K053409
Device Name 3M LIQUID BANDAGE
Applicant
3M COMPANY
3M CENTER, BLDG. 275-5W-06
ST. PAUL,  MN  55144 -1000
Applicant Contact BRYAN BECKER
Correspondent
3M COMPANY
3M CENTER, BLDG. 275-5W-06
ST. PAUL,  MN  55144 -1000
Correspondent Contact BRYAN BECKER
Regulation Number880.5090
Classification Product Code
KMF  
Date Received12/07/2005
Decision Date 06/19/2006
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
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