ZIPPIE & QUICKIE 2HP WHEELCHAIR
K-Number: K890050 · 1989-02-08
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Device Summary
Frequently Asked Questions
What is the ZIPPIE & QUICKIE 2HP WHEELCHAIR?
ZIPPIE & QUICKIE 2HP WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1989-02-08. The listed applicant is Motion Designs, Inc.. The 510(k) number is K890050.
When did ZIPPIE & QUICKIE 2HP WHEELCHAIR receive FDA 510(k) clearance?
ZIPPIE & QUICKIE 2HP WHEELCHAIR received FDA 510(k) clearance on 1989-02-08, under 510(k) number K890050.
Who is the listed applicant for ZIPPIE & QUICKIE 2HP 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 ZIPPIE & QUICKIE 2HP WHEELCHAIR?
The FDA product code for ZIPPIE & QUICKIE 2HP 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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