GOVAN+ WHEELCHAIR AND DOCKING ACCESSORY
K-Number: K011752 · 2001-06-28
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Device Summary
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
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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