meddevicedb.com FDA Device Reference

SERIES 9000 LIFT-RECLINE CHAIR

K903905 Class II Traditional
Decision Date
1990-09-17
Sponsor / Applicant
Equi-Tron Mfg., Inc.

Technical Specification

510(k) Submission ID K903905
Product Code INO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3110
Decision Date 1990-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERIES 9000 LIFT-RECLINE CHAIR received FDA 510(k) clearance under submission number K903905, sponsored by Equi-Tron Mfg., 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 1990-09-17.

Classification & Regulation

This clearance is catalogued under FDA product code INO and 21 CFR 890.3110, within the Physical Medicine review panel as a Class II device.