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

COVERLET ADHESIVE DRESSING

K Number: K940378 · Decision Jul 29, 1994
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
45
Review Days
184

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Basic Information

Device Name
COVERLET ADHESIVE DRESSING
K Number
K940378
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent for Some Indications
Applicant
Beiersdorf, Inc.
Date Received
January 26, 1994
Decision Date
July 29, 1994
Product Code
KGX
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
KGX Tape And Bandage, Adhesive

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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
K925630 ELASTOPLAST HEAT PLASTER
K926399 CUTIFILM(R) FILM
K923404 LUEKOFLEX SURGICAL TAPE
K921759 ACRYLASTIC
Search all 45 clearances from Beiersdorf, Inc. →