3M NO STING BARRIER FILM

Bandage, Liquid

3M MEDICAL PRODUCTS GROUP

The following data is part of a premarket notification filed by 3m Medical Products Group with the FDA for 3m No Sting Barrier Film.

Pre-market Notification Details

Device IDK955103
510k NumberK955103
Device Name:3M NO STING BARRIER FILM
ClassificationBandage, Liquid
Applicant 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul,  MN  55144 -1000
ContactAnna E Mcright
CorrespondentAnna E Mcright
3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul,  MN  55144 -1000
Product CodeKMF  
CFR Regulation Number880.5090 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-11-08
Decision Date1996-02-05

NIH GUDID Devices

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