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FDA 510(k)

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs

K-Number: K181090 · 2018-11-14

Decision Date2018-11-14
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is a medical device manufactured by Invacare Corporation. It received FDA 510(k) clearance on 2018-11-14 under approval number K181090. 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 Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is a medical device that received FDA 510(k) clearance on 2018-11-14. It is manufactured by Invacare Corporation. The 510(k) number is K181090.

When was Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs approved by the FDA?

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs received FDA 510(k) clearance on 2018-11-14, under approval number K181090.

What company makes Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is manufactured by Invacare Corporation.

What is the FDA product code for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?

The FDA product code for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is IOR.

Related Clinical Trials

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Related Devices (Code: IOR)

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.