FDA 510(k)

Mobility Scooter (YL-09B, YL-07)

K-Number: K242139 · 2025-01-06

ApplicantYongkang Yile Vehicle Co., Ltd.

Decision Date2025-01-06

Product CodeINI

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Mobility Scooter (YL-09B, YL-07) is a medical device manufactured by Yongkang Yile Vehicle Co., Ltd.. It received FDA 510(k) clearance on 2025-01-06 under approval number K242139. 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 (YL-09B, YL-07)?

Mobility Scooter (YL-09B, YL-07) is a medical device that received FDA 510(k) clearance on 2025-01-06. It is manufactured by Yongkang Yile Vehicle Co., Ltd.. The 510(k) number is K242139.

When was Mobility Scooter (YL-09B, YL-07) approved by the FDA?

Mobility Scooter (YL-09B, YL-07) received FDA 510(k) clearance on 2025-01-06, under approval number K242139.

What company makes Mobility Scooter (YL-09B, YL-07)?

Mobility Scooter (YL-09B, YL-07) is manufactured by Yongkang Yile Vehicle Co., Ltd..

What is the FDA product code for Mobility Scooter (YL-09B, YL-07)?

The FDA product code for Mobility Scooter (YL-09B, YL-07) is INI.

Other Devices by Yongkang Yile Vehicle Co., Ltd.

K234098Mobility Scooter (C4+)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.