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

ACRYLASTIC

K Number: K921759 · Decision Aug 10, 1992
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
45
Review Days
118

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Basic Information

Device Name
ACRYLASTIC
K Number
K921759
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Beiersdorf, Inc.
Date Received
April 14, 1992
Decision Date
August 10, 1992
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

Similar 510(k) Clearances

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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. →