meddevicedb.com FDA Device Reference

CIE FOLDAWAY WHEELCHAIR

K050345 Class I Traditional
Decision Date
2005-03-29
Sponsor / Applicant
Carlsbad International Export, Inc.

Technical Specification

510(k) Submission ID K050345
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2005-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIE FOLDAWAY WHEELCHAIR received FDA 510(k) clearance under submission number K050345, sponsored by Carlsbad International Export, 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 2005-03-29.

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.