Mobility Scooter (Models: W3431Q, W3431R)
K-Number: K222507 · 2023-02-28
Decision Date2023-02-28
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter (Models: W3431Q, W3431R) is a medical device manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2023-02-28 under approval number K222507. 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 (Models: W3431Q, W3431R)?
Mobility Scooter (Models: W3431Q, W3431R) is a medical device that received FDA 510(k) clearance on 2023-02-28. It is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K222507.
When was Mobility Scooter (Models: W3431Q, W3431R) approved by the FDA?
Mobility Scooter (Models: W3431Q, W3431R) received FDA 510(k) clearance on 2023-02-28, under approval number K222507.
What company makes Mobility Scooter (Models: W3431Q, W3431R)?
Mobility Scooter (Models: W3431Q, W3431R) is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd.
What is the FDA product code for Mobility Scooter (Models: W3431Q, W3431R)?
The FDA product code for Mobility Scooter (Models: W3431Q, W3431R) is INI.
Related Clinical Trials
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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.