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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 K955103
Device Name 3M NO STING BARRIER FILM
Applicant
3M MEDICAL PRODUCTS GROUP
3M CENTER, BLDG. 275-3E-08
ST. PAUL,  MN  55144 -1000
Applicant Contact ANNA E MCRIGHT
Correspondent
3M MEDICAL PRODUCTS GROUP
3M CENTER, BLDG. 275-3E-08
ST. PAUL,  MN  55144 -1000
Correspondent Contact ANNA E MCRIGHT
Regulation Number880.5090
Classification Product Code
KMF  
Date Received11/08/1995
Decision Date 02/05/1996
Decision Substantially Equivalent (SESE)
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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