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

CUTINOVA THIN WOUND DRESSING

K Number: K944581 · Decision Dec 2, 1994
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
221
Applicant Total
45
Review Days
74

Basic Information

Device Name
CUTINOVA THIN WOUND DRESSING
K Number
K944581
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent for Some Indications
Applicant
BEIERSDORF, INC.
Date Received
September 19, 1994
Decision Date
December 2, 1994
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 BEIERSDORF, INC.

K Number Device Name
K090921 ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02
K024057 CURAD SCAR THERAPY
K952526 CUTINOVA CAVITY
K943363 CUTIPLAST STERIL
K935630 NORTA
K940378 COVERLET ADHESIVE DRESSING
K925630 ELASTOPLAST HEAT PLASTER
K926399 CUTIFILM(R) FILM
K923404 LUEKOFLEX SURGICAL TAPE
K921759 ACRYLASTIC
Search all 45 clearances from BEIERSDORF, INC. →