GRAVITY DOWN WHEELCHAIR LIFT
K-Number: K901989 · 1990-05-24
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Device Summary
Frequently Asked Questions
What is the GRAVITY DOWN WHEELCHAIR LIFT?
GRAVITY DOWN WHEELCHAIR LIFT is a medical device that received FDA 510(k) clearance on 1990-05-24. The listed applicant is Crow River Industries, Inc.. The 510(k) number is K901989.
When did GRAVITY DOWN WHEELCHAIR LIFT receive FDA 510(k) clearance?
GRAVITY DOWN WHEELCHAIR LIFT received FDA 510(k) clearance on 1990-05-24, under 510(k) number K901989.
Who is the listed applicant for GRAVITY DOWN 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 GRAVITY DOWN WHEELCHAIR LIFT?
The FDA product code for GRAVITY DOWN 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
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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