meddevicedb.com FDA Device Reference

E Z CHAIR

K993298 Class I Traditional
Decision Date
1999-11-16
Sponsor / Applicant
Premier Designs

Technical Specification

510(k) Submission ID K993298
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 1999-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E Z CHAIR received FDA 510(k) clearance under submission number K993298, sponsored by Premier Designs. 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 1999-11-16.

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.