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

FDA 510(k) K242139 · Yongkang Yile Vehicle Co., Ltd.

Substantially Equivalent

510(k) numberK242139

Submission

Device name
Mobility Scooter (YL-09B, YL-07)
Applicant
Yongkang Yile Vehicle Co., Ltd.
Yongkang, CN
Received
July 22, 2024
Decision date
January 6, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
INI – Vehicle, Motorized 3-Wheeled
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3800
Specialty
Physical Medicine

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More from Nanjing Mijo Technology Co., Ltd.

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K234098Mobility Scooter (C4+)INI · Traditional 04/18/2024SE

Questions and answers

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

Mobility Scooter (YL-09B, YL-07) (K242139) received a 510(k) decision of Substantially Equivalent on January 6, 2025, 168 days after the submission was received.

What is the product code of K242139?

The FDA product code is INI – Vehicle, Motorized 3-Wheeled, a Class II (moderate risk) device regulated under 21 CFR 890.3800.