meddevicedb.com FDA Device Reference

Electric Scooter (Model: S3312)

K230615 Class II Traditional
Decision Date
2023-05-05
Sponsor / Applicant
Guangdong Prestige Technology Co., Ltd.

Technical Specification

510(k) Submission ID K230615
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2023-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electric Scooter (Model: S3312) received FDA 510(k) clearance under submission number K230615, sponsored by Guangdong Prestige Technology 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 2023-05-05.

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.