meddevicedb.com FDA Device Reference

KYMCO FORU, MODEL EQ20

K082901 Class II Traditional
Decision Date
2008-10-28
Sponsor / Applicant
Kwang Yang Motor Co., Ltd.

Technical Specification

510(k) Submission ID K082901
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2008-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KYMCO FORU, MODEL EQ20 received FDA 510(k) clearance under submission number K082901, sponsored by Kwang Yang Motor 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 2008-10-28.

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.