meddevicedb.com FDA Device Reference

Electric Wheelchair (Y207BL)

K253241 Class II Traditional
Decision Date
2026-05-13
Sponsor / Applicant
Jiangsu Intco Medical Products Co., Ltd.

Technical Specification

510(k) Submission ID K253241
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2026-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Wheelchair (Y207BL) received FDA 510(k) clearance under submission number K253241, sponsored by Jiangsu Intco Medical Products 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 2026-05-13.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.