meddevicedb.com FDA Device Reference

Walking rehabilitation training electric wheelchair (ZW518)

K243783 Class II Traditional
Decision Date
2025-03-12
Sponsor / Applicant
Shenzhen Zuowei Technology Co., Ltd.

Technical Specification

510(k) Submission ID K243783
Product Code IPL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3900
Decision Date 2025-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Walking rehabilitation training electric wheelchair (ZW518) received FDA 510(k) clearance under submission number K243783, sponsored by Shenzhen Zuowei 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 2025-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code IPL and 21 CFR 890.3900, within the Physical Medicine review panel as a Class II device.