QUICKIE QX MANUAL FOLDING WHEELCHAIR
K-Number: K072153 · 2007-09-10
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Device Summary
Frequently Asked Questions
What is the QUICKIE QX MANUAL FOLDING WHEELCHAIR?
QUICKIE QX MANUAL FOLDING WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2007-09-10. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K072153.
When did QUICKIE QX MANUAL FOLDING WHEELCHAIR receive FDA 510(k) clearance?
QUICKIE QX MANUAL FOLDING WHEELCHAIR received FDA 510(k) clearance on 2007-09-10, under 510(k) number K072153.
Who is the listed applicant for QUICKIE QX MANUAL FOLDING WHEELCHAIR?
The FDA 510(k) record lists Sunrise Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUICKIE QX MANUAL FOLDING WHEELCHAIR?
The FDA product code for QUICKIE QX MANUAL FOLDING 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 Sunrise Medical, 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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