meddevicedb.com FDA Device Reference

RESUBMITTED ERGOMETER EXERCISE BIKE MODEL FT1300

K880865 Class I Traditional
Decision Date
1988-05-02
Sponsor / Applicant
Invacare Corp.

Technical Specification

510(k) Submission ID K880865
Product Code BXB
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1988-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RESUBMITTED ERGOMETER EXERCISE BIKE MODEL FT1300 received FDA 510(k) clearance under submission number K880865, 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 1988-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code BXB and 21 CFR 890.5380, within the Physical Medicine review panel as a Class I device.