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

LEUKOCLIP(R)

K Number: K873744 · Decision Sep 30, 1987
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
5
Applicant Total
45
Review Days
14

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Basic Information

Device Name
LEUKOCLIP(R)
K Number
K873744
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4320
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Beiersdorf, Inc.
Date Received
September 16, 1987
Decision Date
September 30, 1987
Product Code
FZQ
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
FZQ Clip, Removable (Skin)

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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. →