QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR
K-Number: K982989 · 1998-10-05
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Device Summary
Frequently Asked Questions
What is the QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR?
QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Sunrise Medical, Inc.. The 510(k) number is K982989.
When did QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR receive FDA 510(k) clearance?
QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR received FDA 510(k) clearance on 1998-10-05, under 510(k) number K982989.
Who is the listed applicant for QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR?
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 SUSPENSION WHEELCHAIR SERIES MODEL XTR?
The FDA product code for QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR 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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