Mobility Scooter (C4+)
K-Number: K234098 · 2024-04-18
ApplicantYongkang Yile Vehicle Co., Ltd.
Decision Date2024-04-18
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter (C4+) is a medical device manufactured by Yongkang Yile Vehicle Co., Ltd.. It received FDA 510(k) clearance on 2024-04-18 under approval number K234098. 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 (C4+)?
Mobility Scooter (C4+) is a medical device that received FDA 510(k) clearance on 2024-04-18. It is manufactured by Yongkang Yile Vehicle Co., Ltd.. The 510(k) number is K234098.
When was Mobility Scooter (C4+) approved by the FDA?
Mobility Scooter (C4+) received FDA 510(k) clearance on 2024-04-18, under approval number K234098.
What company makes Mobility Scooter (C4+)?
Mobility Scooter (C4+) is manufactured by Yongkang Yile Vehicle Co., Ltd..
What is the FDA product code for Mobility Scooter (C4+)?
The FDA product code for Mobility Scooter (C4+) is INI.
Other Devices by Yongkang Yile Vehicle 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.