Caregiver-assisted wheelchair (MS02);Caregiver-assisted wheelchair (MA02)

FDA 510(k) K261076 · GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.

Substantially Equivalent

510(k) numberK261076

Submission

Device name
Caregiver-assisted wheelchair (MS02);Caregiver-assisted wheelchair (MA02)
Applicant
GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.
Zhongshan, CN
Received
April 1, 2026
Decision date
June 22, 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
IOR – Wheelchair, Mechanical
Device class
Class I (low risk)
Regulation
21 CFR 890.3850
Specialty
Physical Medicine

A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position” to mean the device type is intended to provide mobility to individuals who have mobility impairments and/or require an assistive device for mobility.

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More from Jiangsu Jumao X-Care Medical Equipment Co., , Ltd.

510(k)DeviceDecision
K261075Manual Wheelchair (MS01);Manual Wheelchair (MA01)IOR · Traditional 06/22/2026SE

Questions and answers

When was Caregiver-assisted wheelchair (MS02);Caregiver-assisted wheelchair (MA02) cleared by the FDA?

Caregiver-assisted wheelchair (MS02);Caregiver-assisted wheelchair (MA02) (K261076) received a 510(k) decision of Substantially Equivalent on June 22, 2026, 82 days after the submission was received.

What is the product code of K261076?

The FDA product code is IOR – Wheelchair, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3850.