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FDA 510(k)

ULTRAGATER WHEELCHAIR LIFT

K-Number: K922624 · 1992-07-13

Decision Date1992-07-13
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ULTRAGATER WHEELCHAIR LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Crow River Industries, Inc.. It received FDA 510(k) clearance on 1992-07-13 under 510(k) number K922624. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRAGATER WHEELCHAIR LIFT?

ULTRAGATER WHEELCHAIR LIFT is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Crow River Industries, Inc.. The 510(k) number is K922624.

When did ULTRAGATER WHEELCHAIR LIFT receive FDA 510(k) clearance?

ULTRAGATER WHEELCHAIR LIFT received FDA 510(k) clearance on 1992-07-13, under 510(k) number K922624.

Who is the listed applicant for ULTRAGATER WHEELCHAIR LIFT?

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

What is the FDA product code for ULTRAGATER WHEELCHAIR LIFT?

The FDA product code for ULTRAGATER WHEELCHAIR LIFT is ING.

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 Crow River Industries, Inc. 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: ING)

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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