QUICKIE RX PRESCRIPTION WHEELCHAIR
K-Number: K870476 · 1987-02-26
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Device Summary
Frequently Asked Questions
What is the QUICKIE RX PRESCRIPTION WHEELCHAIR?
QUICKIE RX PRESCRIPTION WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1987-02-26. The listed applicant is Motion Designs, Inc.. The 510(k) number is K870476.
When did QUICKIE RX PRESCRIPTION WHEELCHAIR receive FDA 510(k) clearance?
QUICKIE RX PRESCRIPTION WHEELCHAIR received FDA 510(k) clearance on 1987-02-26, under 510(k) number K870476.
Who is the listed applicant for QUICKIE RX PRESCRIPTION WHEELCHAIR?
The FDA 510(k) record lists Motion Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUICKIE RX PRESCRIPTION WHEELCHAIR?
The FDA product code for QUICKIE RX PRESCRIPTION WHEELCHAIR is IOR.
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 Motion Designs, 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: IOR)
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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