meddevicedb.com FDA Device Reference

TMX-70 TREADMILL

K851629 Class I Traditional
Decision Date
1985-07-09
Sponsor / Applicant
Eaton Medical Group

Technical Specification

510(k) Submission ID K851629
Product Code IOL
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5380
Decision Date 1985-07-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TMX-70 TREADMILL received FDA 510(k) clearance under submission number K851629, sponsored by Eaton Medical Group. 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 1985-07-09.

Classification & Regulation

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