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

AIRCAST VENAFLOW SYSTEM

K Number: K932900 · Decision Oct 25, 1993
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
11
Review Days
133

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Basic Information

Device Name
AIRCAST VENAFLOW SYSTEM
K Number
K932900
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Aircast, Inc.
Date Received
June 14, 1993
Decision Date
October 25, 1993
Product Code
JOW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
JOW Sleeve, Limb, Compressible

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Other Clearances by Aircast, Inc.

K Number Device Name
K024019 ARTERIALFLOW SYSTEM, MODEL 32A
K023800 VENAFLOW REUSABLE CALF AIRCELL, MODEL 3018, VENAFLOW DISPOSABLE CALF COVER, MODEL 3017
K992454 VENAFLOW SYSTEM, MODEL 30A
K964238 AIRCAST VENA FLOW STERILE DISPOSABLE CUFFS
K961676 AIRCAST VENAFLOW SYSTEM (MODIFICATION)
K933977 AIRCAST EDEMAFLOW SYSTEM
K925677 AUTOCHILL ACCESSORY KIT
K812094 AIRCAST PNEUMATIC KNEE BRACE
K810288 AIRCAST TENNIS ARM BAND
K780979 AIRSTIRRUP PNEUMATIC ANKLE BRACE
Search all 11 clearances from Aircast, Inc. →