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FDA 510(k)

KARMA 800 SERIES MANUAL WHEELCHAIR

K-Number: K021866 · 2002-06-14

Decision Date2002-06-14
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KARMA 800 SERIES MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Vestil Manufacturing Corp.. It received FDA 510(k) clearance on 2002-06-14 under 510(k) number K021866. 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 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

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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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