meddevicedb.com FDA Device Reference

Electric Wheelchair (Robooter E40), Model name: BBR-E40-01

K231868 Class II Traditional
Decision Date
2023-10-31
Sponsor / Applicant
Shanghai Bangbang Robotics Co., Ltd.

Technical Specification

510(k) Submission ID K231868
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2023-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Wheelchair (Robooter E40), Model name: BBR-E40-01 received FDA 510(k) clearance under submission number K231868, sponsored by Shanghai Bangbang Robotics 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 2023-10-31.

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.