WHEELCHAIR LIFT (WHEELCHAIR ELEVATOR)
K-Number: K900417 · 1990-02-15
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Device Summary
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
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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