meddevicedb.com FDA Device Reference

GEN_2 and GEN_3 Mechanical Wheelchairs

K170701 Class I Special
Decision Date
2017-03-24
Sponsor / Applicant
Free Wheelchair Mission

Technical Specification

510(k) Submission ID K170701
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2017-03-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GEN_2 and GEN_3 Mechanical Wheelchairs received FDA 510(k) clearance under submission number K170701, sponsored by Free Wheelchair Mission. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2017-03-24.

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.