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FDA 510(k)

GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY

K-Number: K011752 · 2001-06-28

Decision Date2001-06-28
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Accufast, Inc.. It received FDA 510(k) clearance on 2001-06-28 under 510(k) number K011752. 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 GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY?

GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY is a medical device that received FDA 510(k) clearance on 2001-06-28. The listed applicant is Accufast, Inc.. The 510(k) number is K011752.

When did GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY receive FDA 510(k) clearance?

GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY received FDA 510(k) clearance on 2001-06-28, under 510(k) number K011752.

Who is the listed applicant for GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY?

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

What is the FDA product code for GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY?

The FDA product code for GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY 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.

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

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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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