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

CUTINOVA GELFILM SYNTHETIC WOUND DRESSING, STERILE

K Number: K850147 · Decision Jul 5, 1985
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
45
Review Days
172

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Basic Information

Device Name
CUTINOVA GELFILM SYNTHETIC WOUND DRESSING, STERILE
K Number
K850147
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Beiersdorf, Inc.
Date Received
January 14, 1985
Decision Date
July 5, 1985
Product Code
FRO
Advisory Committee
Unknown
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
FRO Dressing, Wound, Drug

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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
K944581 CUTINOVA THIN WOUND DRESSING
K935630 NORTA
K940378 COVERLET ADHESIVE DRESSING
K925630 ELASTOPLAST HEAT PLASTER
K926399 CUTIFILM(R) FILM
K923404 LUEKOFLEX SURGICAL TAPE
Search all 45 clearances from Beiersdorf, Inc. →