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FDA 510(k)

ACTION AT MANUAL WHEELCHAIR

K-Number: K941989 · 1994-05-11

ApplicantNvacare Corp.
Decision Date1994-05-11
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACTION AT MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Nvacare Corp.. It received FDA 510(k) clearance on 1994-05-11 under 510(k) number K941989. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTION AT MANUAL WHEELCHAIR?

ACTION AT MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1994-05-11. The listed applicant is Nvacare Corp.. The 510(k) number is K941989.

When did ACTION AT MANUAL WHEELCHAIR receive FDA 510(k) clearance?

ACTION AT MANUAL WHEELCHAIR received FDA 510(k) clearance on 1994-05-11, under 510(k) number K941989.

Who is the listed applicant for ACTION AT MANUAL WHEELCHAIR?

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

What is the FDA product code for ACTION AT MANUAL WHEELCHAIR?

The FDA product code for ACTION AT MANUAL WHEELCHAIR is IOR.

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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.

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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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