Cleared Traditional

Manual Wheelchair (W50)

K253632 · Jiangsu Jumao X-Care Medical Equipment Co., Ltd. · Physical Medicine

Jan 2026

Decision

71d

Days

Class 1

Risk

About This 510(k) Submission

K253632 is an FDA 510(k) clearance for the Manual Wheelchair (W50), a Wheelchair, Mechanical (Class I — General Controls, product code IOR), submitted by Jiangsu Jumao X-Care Medical Equipment Co., Ltd. (Danyang, CN). The FDA issued a Cleared decision on January 29, 2026, 71 days after receiving the submission on November 19, 2025. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3850.

Submission Details

510(k) Number	K253632 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 19, 2025
Decision Date	January 29, 2026
Days to Decision	71 days
Submission Type	Traditional
Review Panel	Physical Medicine (PM)
Summary	Summary PDF

Device Classification

Product Code	IOR — Wheelchair, Mechanical
Device Class	Class I — General Controls
CFR Regulation	21 CFR 890.3850
Definition	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.