KARMA 800 SERIES MANUAL WHEELCHAIR
K-Number: K021866 · 2002-06-14
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Device Summary
Frequently Asked Questions
What is the KARMA 800 SERIES MANUAL WHEELCHAIR?
KARMA 800 SERIES MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2002-06-14. The listed applicant is Vestil Manufacturing Corp.. The 510(k) number is K021866.
When did KARMA 800 SERIES MANUAL WHEELCHAIR receive FDA 510(k) clearance?
KARMA 800 SERIES MANUAL WHEELCHAIR received FDA 510(k) clearance on 2002-06-14, under 510(k) number K021866.
Who is the listed applicant for KARMA 800 SERIES MANUAL WHEELCHAIR?
The FDA 510(k) record lists Vestil Manufacturing Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARMA 800 SERIES MANUAL WHEELCHAIR?
The FDA product code for KARMA 800 SERIES MANUAL 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 Vestil Manufacturing 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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