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FDA 510(k)

SOLARA JR. MANUAL WHEELCHAIR

K-Number: K012370 · 2001-08-03

Decision Date2001-08-03
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SOLARA JR. MANUAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 2001-08-03 under 510(k) number K012370. 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 SOLARA JR. MANUAL WHEELCHAIR?

SOLARA JR. MANUAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 2001-08-03. The listed applicant is Invacare Corp.. The 510(k) number is K012370.

When did SOLARA JR. MANUAL WHEELCHAIR receive FDA 510(k) clearance?

SOLARA JR. MANUAL WHEELCHAIR received FDA 510(k) clearance on 2001-08-03, under 510(k) number K012370.

Who is the listed applicant for SOLARA JR. MANUAL WHEELCHAIR?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLARA JR. MANUAL WHEELCHAIR?

The FDA product code for SOLARA JR. MANUAL 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 Invacare Corp. 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 111 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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