meddevicedb.com FDA Device Reference

HYPERTHERM TECHNOLOGIES' HEAT COMPRESS

K873364 Class I Traditional
Decision Date
1987-11-17
Sponsor / Applicant
Hypertherm Technologies, Inc.

Technical Specification

510(k) Submission ID K873364
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1987-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYPERTHERM TECHNOLOGIES' HEAT COMPRESS received FDA 510(k) clearance under submission number K873364, sponsored by Hypertherm Technologies, 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 1987-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code IMD and 21 CFR 890.5710, within the Physical Medicine review panel as a Class I device.