ACTION AF-1 WHEELCHAIR
K-Number: K000174 · 2000-02-18
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Device Summary
Frequently Asked Questions
What is the ACTION AF-1 WHEELCHAIR?
ACTION AF-1 WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2000-02-18. The listed applicant is Invacare Corp.. The 510(k) number is K000174.
When did ACTION AF-1 WHEELCHAIR receive FDA 510(k) clearance?
ACTION AF-1 WHEELCHAIR received FDA 510(k) clearance on 2000-02-18, under 510(k) number K000174.
Who is the listed applicant for ACTION AF-1 WHEELCHAIR?
The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACTION AF-1 WHEELCHAIR?
The FDA product code for ACTION AF-1 WHEELCHAIR is IOR.
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 Invacare Corp. 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: IOR)
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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