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. The listed applicant is Invacare Corporation. The 510(k) number is K181090.
When did Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs receive FDA 510(k) clearance?
Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs received FDA 510(k) clearance on 2018-11-14, under 510(k) number K181090.
Who is the listed applicant for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?
The FDA 510(k) record lists Invacare Corporation as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Invacare Corporation 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.