FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

VENOTRAIN CURAFLOW

K Number: K111662 · Decision Oct 4, 2011
Classifications
1
FEI Numbers
91
Registration Numbers
91
Same Product Code
63
Applicant Total
2
Review Days
112

Basic Information

Device Name
VENOTRAIN CURAFLOW
K Number
K111662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5780
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BAUERFEIND AG
Date Received
June 14, 2011
Decision Date
October 4, 2011
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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K Number Device Name
K123921 BODYTRONIC 200