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

ARTIFLEX(TM)

K Number: K910274 · Decision Mar 5, 1991
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
30
Applicant Total
45
Review Days
41

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Basic Information

Device Name
ARTIFLEX(TM)
K Number
K910274
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.5940
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Beiersdorf, Inc.
Date Received
January 23, 1991
Decision Date
March 5, 1991
Product Code
LGF
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LGF Component, Cast

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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
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