meddevicedb.com FDA Device Reference

FORYOU POWERED WHEELCHAIR, MODEL FC-100

K061693 Class II Traditional
Decision Date
2006-07-06
Sponsor / Applicant
Foryou Technology Co., Ltd.

Technical Specification

510(k) Submission ID K061693
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2006-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FORYOU POWERED WHEELCHAIR, MODEL FC-100 received FDA 510(k) clearance under submission number K061693, sponsored by Foryou 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 2006-07-06.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.