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

ARTERIALFLOW SYSTEM, MODEL 32A

K Number: K024019 · Decision Jun 3, 2003
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
11
Review Days
180

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Basic Information

Device Name
ARTERIALFLOW SYSTEM, MODEL 32A
K Number
K024019
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
December 5, 2002
Decision Date
June 3, 2003
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
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K964238 AIRCAST VENA FLOW STERILE DISPOSABLE CUFFS
K961676 AIRCAST VENAFLOW SYSTEM (MODIFICATION)
K933977 AIRCAST EDEMAFLOW SYSTEM
K932900 AIRCAST VENAFLOW SYSTEM
K925677 AUTOCHILL ACCESSORY KIT
K812094 AIRCAST PNEUMATIC KNEE BRACE
K810288 AIRCAST TENNIS ARM BAND
K780979 AIRSTIRRUP PNEUMATIC ANKLE BRACE
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