Mobility Scooter, Model: W3331F
K-Number: K222495 · 2022-10-17
Decision Date2022-10-17
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter, Model: W3331F is a medical device manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2022-10-17 under approval number K222495. 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, Model: W3331F?
Mobility Scooter, Model: W3331F is a medical device that received FDA 510(k) clearance on 2022-10-17. It is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K222495.
When was Mobility Scooter, Model: W3331F approved by the FDA?
Mobility Scooter, Model: W3331F received FDA 510(k) clearance on 2022-10-17, under approval number K222495.
What company makes Mobility Scooter, Model: W3331F?
Mobility Scooter, Model: W3331F is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd.
What is the FDA product code for Mobility Scooter, Model: W3331F?
The FDA product code for Mobility Scooter, Model: W3331F 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.