meddevicedb.com FDA Device Reference

Therm-X Pro, Therm-X AT, Therm-X Pro Athlete

K181149 Class II Traditional
Decision Date
2018-08-03
Sponsor / Applicant
Zenith Technical Innovations

Technical Specification

510(k) Submission ID K181149
Product Code IRP
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5650
Decision Date 2018-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Therm-X Pro, Therm-X AT, Therm-X Pro Athlete received FDA 510(k) clearance under submission number K181149, sponsored by Zenith Technical Innovations. 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 2018-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code IRP and 21 CFR 890.5650, within the Physical Medicine review panel as a Class II device.