ARTERIALFLOW SYSTEM, MODEL 32A
K-Number: K024019 · 2003-06-03
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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