meddevicedb.com FDA Device Reference

i3 Foldable Mobility Scooter

K191356 Class II Traditional
Decision Date
2022-01-11
Sponsor / Applicant
Puc Perfect Union Co., Ltd.

Technical Specification

510(k) Submission ID K191356
Product Code INI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3800
Decision Date 2022-01-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

i3 Foldable Mobility Scooter received FDA 510(k) clearance under submission number K191356, sponsored by Puc Perfect Union 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 2022-01-11.

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.