meddevicedb.com FDA Device Reference

Electric Scooter

K212090 Class II Traditional
Decision Date
2022-04-22
Sponsor / Applicant
Anhui Jbh Medical Apparatus Co., Ltd.

Technical Specification

510(k) Submission ID K212090
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2022-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Scooter received FDA 510(k) clearance under submission number K212090, sponsored by Anhui Jbh Medical Apparatus 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 2022-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code INI and 21 CFR 890.3800, within the Physical Medicine review panel as a Class II device.