meddevicedb.com FDA Device Reference

ZIP'R4/ ZIP'R4 XTRA SCOOTER

K102361 Class II Traditional
Decision Date
2010-10-04
Sponsor / Applicant
Global Fabtech Wheelchair (Shanghai) Co., Ltd.

Technical Specification

510(k) Submission ID K102361
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2010-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZIP'R4/ ZIP'R4 XTRA SCOOTER received FDA 510(k) clearance under submission number K102361, sponsored by Global Fabtech Wheelchair (Shanghai) 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 2010-10-04.

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.