meddevicedb.com FDA Device Reference

QUICKIE QX MANUAL FOLDING WHEELCHAIR

K072153 Class I Traditional
Decision Date
2007-09-10
Sponsor / Applicant
Sunrise Medical, Inc.

Technical Specification

510(k) Submission ID K072153
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2007-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICKIE QX MANUAL FOLDING WHEELCHAIR received FDA 510(k) clearance under submission number K072153, sponsored by Sunrise Medical, Inc.. 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 2007-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.