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

COVER-ROLL STRETCH

K Number: K823879 · Decision Mar 9, 1983
Classifications
1
FEI Numbers
570
Registration Numbers
570
Same Product Code
87
Applicant Total
45
Review Days
72

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Basic Information

Device Name
COVER-ROLL STRETCH
K Number
K823879
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4014
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Beiersdorf, Inc.
Date Received
December 27, 1982
Decision Date
March 9, 1983
Product Code
NAB
Advisory Committee
General, Plastic Surgery
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
NAB Gauze / Sponge,Nonresorbable For External Use

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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. →