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FDA 510(k)

ARTERIALFLOW SYSTEM, MODEL 32A

K-Number: K024019 · 2003-06-03

ApplicantAircast, Inc.
Decision Date2003-06-03
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTERIALFLOW SYSTEM, MODEL 32A is the device name listed in this FDA 510(k) record. The listed applicant is Aircast, Inc.. It received FDA 510(k) clearance on 2003-06-03 under 510(k) number K024019. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIALFLOW SYSTEM, MODEL 32A?

ARTERIALFLOW SYSTEM, MODEL 32A is a medical device that received FDA 510(k) clearance on 2003-06-03. The listed applicant is Aircast, Inc.. The 510(k) number is K024019.

When did ARTERIALFLOW SYSTEM, MODEL 32A receive FDA 510(k) clearance?

ARTERIALFLOW SYSTEM, MODEL 32A received FDA 510(k) clearance on 2003-06-03, under 510(k) number K024019.

Who is the listed applicant for ARTERIALFLOW SYSTEM, MODEL 32A?

The FDA 510(k) record lists Aircast, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTERIALFLOW SYSTEM, MODEL 32A?

The FDA product code for ARTERIALFLOW SYSTEM, MODEL 32A is JOW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Aircast, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 11 devices →

Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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