Mobility Scooter
K-Number: K220206 · 2022-03-24
Decision Date2022-03-24
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter is a medical device manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2022-03-24 under approval number K220206. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Mobility Scooter?
Mobility Scooter is a medical device that received FDA 510(k) clearance on 2022-03-24. It is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K220206.
When was Mobility Scooter approved by the FDA?
Mobility Scooter received FDA 510(k) clearance on 2022-03-24, under approval number K220206.
What company makes Mobility Scooter?
Mobility Scooter is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd.
What is the FDA product code for Mobility Scooter?
The FDA product code for Mobility Scooter is INI.
Other Devices by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd
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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.