Manual Wheelchair (H008, PCK7)

FDA 510(k) K261571 · Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

Substantially Equivalent

510(k) numberK261571

Submission

Device name
Manual Wheelchair (H008, PCK7)
Applicant
Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.
Danyang Jiangsu, CN
Received
May 12, 2026
Decision date
August 6, 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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Questions and answers

When was Manual Wheelchair (H008, PCK7) cleared by the FDA?

Manual Wheelchair (H008, PCK7) (K261571) received a 510(k) decision of Substantially Equivalent on August 6, 2026, 86 days after the submission was received.

What is the product code of K261571?

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