meddevicedb.com FDA Device Reference

RENEGADE WHEELCHAIR

K082857 Class II Traditional
Decision Date
2009-01-06
Sponsor / Applicant
Alpha One

Technical Specification

510(k) Submission ID K082857
Product Code IQC
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3880
Decision Date 2009-01-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RENEGADE WHEELCHAIR received FDA 510(k) clearance under submission number K082857, sponsored by Alpha One. 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 2009-01-06.

Classification & Regulation

This clearance is catalogued under FDA product code IQC and 21 CFR 890.3880, within the Physical Medicine review panel as a Class II device.