FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02

K Number: K090921 · Decision Dec 18, 2009
Classifications
1
FEI Numbers
99
Registration Numbers
99
Same Product Code
63
Applicant Total
45
Review Days
261

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Basic Information

Device Name
ANTI-EMBOLISM STOCKINGS, MODELS 71055-00000-02, 71057-00000-02, 71059-00000-02, 71064-00000-02 & 71065-00000-02
K Number
K090921
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5780
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beiersdorf, Inc.
Date Received
April 1, 2009
Decision Date
December 18, 2009
Product Code
DWL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
DWL Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)

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Other Clearances by Beiersdorf, Inc.

K Number Device Name
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
K921759 ACRYLASTIC
Search all 45 clearances from Beiersdorf, Inc. →