meddevicedb.com FDA Device Reference

Manual Wheelchair (W50)

K253632 Class I Traditional
Decision Date
2026-01-29
Sponsor / Applicant
Jiangsu Jumao X-Care Medical Equipment Co., , Ltd.

Technical Specification

510(k) Submission ID K253632
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2026-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Manual Wheelchair (W50) received FDA 510(k) clearance under submission number K253632, sponsored by Jiangsu Jumao X-Care Medical Equipment Co., , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2026-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.