Mobility Scooter (R200)

FDA 510(k) K261163 · Yongkang Ruihe Metal Product Co., Ltd.

Substantially Equivalent

510(k) numberK261163

Submission

Device name
Mobility Scooter (R200)
Applicant
Yongkang Ruihe Metal Product Co., Ltd.
Yongkang, CN
Received
April 9, 2026
Decision date
July 7, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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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K252813Electrical Scooter (SM4226)INI · Traditional Lerado Zhongshan Peaceful Cove Business Trading…03/17/2026SE
K253936Power Mobility Scooter (MJMA01, MJMA02)INI · Traditional Nanjing Mijo Technology Co., Ltd.03/12/2026SE
K253631Mobility Scooter (CL-Q3, CL-Q4)INI · Traditional Zhejiang Wei Ling New Energy Technology Co., Ltd.02/23/2026SE

More from Zhejiang Wei Ling New Energy Technology Co., Ltd.

510(k)DeviceDecision
K261164Electric wheelchair (XW-LY007 )ITI · Traditional 07/07/2026SE

Questions and answers

When was Mobility Scooter (R200) cleared by the FDA?

Mobility Scooter (R200) (K261163) received a 510(k) decision of Substantially Equivalent on July 7, 2026, 89 days after the submission was received.

What is the product code of K261163?

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