meddevicedb.com FDA Device Reference

MODEL 9000 BARIATRIC WHEELCHAIR

K002317 Class I Traditional
Decision Date
2000-08-25
Sponsor / Applicant
Invacare Corp.

Technical Specification

510(k) Submission ID K002317
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2000-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 9000 BARIATRIC WHEELCHAIR received FDA 510(k) clearance under submission number K002317, sponsored by Invacare Corp.. 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 2000-08-25.

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.