ARTERIALFLOW SYSTEM, MODEL 32A— 510(k) K024019

Substantially Equivalent

Aircast, Inc.

FDA 510(k) clearance K024019 for ARTERIALFLOW SYSTEM, MODEL 32A, Substantially Equivalent on 2003-06-03. Applicant: Aircast, Inc.. Device class: 2.

Clearance details

Applicant: Aircast, Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2002-12-05
Decision date: 2003-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Summit, NJ, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.