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FDA 510(k)

WHEELCHAIR, MODELS H001A, 4422

K-Number: K000738 · 2000-05-26

ApplicantJackson Company, LLC
Decision Date2000-05-26
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR, MODELS H001A, 4422 is the device name listed in this FDA 510(k) record. The listed applicant is Jackson Company, LLC. It received FDA 510(k) clearance on 2000-05-26 under 510(k) number K000738. 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 WHEELCHAIR, MODELS H001A, 4422?

WHEELCHAIR, MODELS H001A, 4422 is a medical device that received FDA 510(k) clearance on 2000-05-26. The listed applicant is Jackson Company, LLC. The 510(k) number is K000738.

When did WHEELCHAIR, MODELS H001A, 4422 receive FDA 510(k) clearance?

WHEELCHAIR, MODELS H001A, 4422 received FDA 510(k) clearance on 2000-05-26, under 510(k) number K000738.

Who is the listed applicant for WHEELCHAIR, MODELS H001A, 4422?

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

What is the FDA product code for WHEELCHAIR, MODELS H001A, 4422?

The FDA product code for WHEELCHAIR, MODELS H001A, 4422 is IOR.

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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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