Mobility Scooter (N3473)
K-Number: K242387 · 2024-10-11
Decision Date2024-10-11
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter (N3473) is a medical device manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2024-10-11 under approval number K242387. 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 (N3473)?
Mobility Scooter (N3473) is a medical device that received FDA 510(k) clearance on 2024-10-11. It is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K242387.
When was Mobility Scooter (N3473) approved by the FDA?
Mobility Scooter (N3473) received FDA 510(k) clearance on 2024-10-11, under approval number K242387.
What company makes Mobility Scooter (N3473)?
Mobility Scooter (N3473) is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd.
What is the FDA product code for Mobility Scooter (N3473)?
The FDA product code for Mobility Scooter (N3473) 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.