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

CUTIPLAST STERIL

K Number: K943363 · Decision Mar 15, 1995
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
79
Applicant Total
45
Review Days
245

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Basic Information

Device Name
CUTIPLAST STERIL
K Number
K943363
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beiersdorf, Inc.
Date Received
July 13, 1994
Decision Date
March 15, 1995
Product Code
MGP
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
MGP Dressing, Wound And Burn, Occlusive

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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
K944581 CUTINOVA THIN WOUND DRESSING
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. →