meddevicedb.com FDA Device Reference

Electric Wheelchair (MP201C); Electric Wheelchair (MP201L)

K241463 Class II Traditional
Decision Date
2024-07-18
Sponsor / Applicant
Suzhou Master Machinery Manufacturing Co.,Ltd

Technical Specification

510(k) Submission ID K241463
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2024-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Wheelchair (MP201C); Electric Wheelchair (MP201L) received FDA 510(k) clearance under submission number K241463, sponsored by Suzhou Master Machinery Manufacturing 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 2024-07-18.

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.