meddevicedb.com FDA Device Reference

HOT/ICE

K830757 Class II Traditional
Decision Date
1983-03-29
Sponsor / Applicant
Thermo Temp, Inc.

Technical Specification

510(k) Submission ID K830757
Product Code ILO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5720
Decision Date 1983-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOT/ICE received FDA 510(k) clearance under submission number K830757, sponsored by Thermo Temp, Inc.. 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 1983-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code ILO and 21 CFR 890.5720, within the Physical Medicine review panel as a Class II device.