Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs
K-Number: K181090 · 2018-11-14
Device Summary
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
Other Devices by Invacare Corporation
Related Devices (Code: IOR)
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.