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FDA 510(k)

QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR

K-Number: K982989 · 1998-10-05

Decision Date1998-10-05
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

QUICKIE SUSPENSION WHEELCHAIR SERIES MODEL XTR is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical, Inc.. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K982989. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 19 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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