meddevicedb.com FDA Device Reference

Electric Wheelchair (Model P2)

K252428 Class II Traditional
Decision Date
2025-09-18
Sponsor / Applicant
Superpi Robot Co., Ltd.

Technical Specification

510(k) Submission ID K252428
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2025-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Wheelchair (Model P2) received FDA 510(k) clearance under submission number K252428, sponsored by Superpi Robot 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 2025-09-18.

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.