meddevicedb.com FDA Device Reference

Weely Manual Wheelchair

K152827 Class I Traditional
Decision Date
2016-02-19
Sponsor / Applicant
Rupiani

Technical Specification

510(k) Submission ID K152827
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2016-02-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Weely Manual Wheelchair received FDA 510(k) clearance under submission number K152827, sponsored by Rupiani. 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 2016-02-19.

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.