FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

3M NO STING BARRIER FILM

K Number: K955103 · Decision Feb 5, 1996
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
12
Review Days
89

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
3M NO STING BARRIER FILM
K Number
K955103
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M Medical Products Group
Date Received
November 8, 1995
Decision Date
February 5, 1996
Product Code
KMF
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KMF Bandage, Liquid

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KMF), ordered by most recent decision date.

View all

Other Clearances by 3M Medical Products Group

K Number Device Name
K971444 3M RED DOT 2234 & 2266 RADIOLUCENT MONITORING ELECTRODES
K952121 3M RESIN CEMENT
K945726 3M(TM) EAR IMPRESSION MATERIAL
K941718 3M FLUID CONTROL SYSTEM 8300 CASSETTE LOAD
K934333 3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE
K923222 3M COLOR LASER IMAGER, MODEL 979
K923075 3M LASER IMAGER MODEL 969
K911252 PRECISE BARND PI DISPOSABLE SURGICAL STAPLES
K912225 3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT
K910092 3M LASER IMAGER XL
Search all 12 clearances from 3M Medical Products Group →