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FDA 510(k)

WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR)

K-Number: K900417 · 1990-02-15

Decision Date1990-02-15
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR) 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 1990-02-15 under 510(k) number K900417. 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 WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR)?

WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR) is a medical device that received FDA 510(k) clearance on 1990-02-15. The listed applicant is Crow River Industries, Inc.. The 510(k) number is K900417.

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

WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR) received FDA 510(k) clearance on 1990-02-15, under 510(k) number K900417.

Who is the listed applicant for WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR)?

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 WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR)?

The FDA product code for WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR) 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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