meddevicedb.com FDA Device Reference

Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP

K192216 Class II Traditional
Decision Date
2020-01-02
Sponsor / Applicant
Invacare Corporation

Technical Specification

510(k) Submission ID K192216
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2020-01-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP received FDA 510(k) clearance under submission number K192216, sponsored by Invacare Corporation. 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 2020-01-02.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.