meddevicedb.com FDA Device Reference

Aluminum back folding wheelchair SYIV 100-LQXAL2482-407

K213790 Class I Traditional
Decision Date
2022-03-14
Sponsor / Applicant
Mobility Source Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K213790
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2022-03-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Aluminum back folding wheelchair SYIV 100-LQXAL2482-407 received FDA 510(k) clearance under submission number K213790, sponsored by Mobility Source Medical Technology 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 2022-03-14.

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.