meddevicedb.com FDA Device Reference

WARM-EE HEAT PACK

K791684 Class I Traditional
Decision Date
1979-10-30
Sponsor / Applicant
U.S. Export Marketing Group, Inc.

Technical Specification

510(k) Submission ID K791684
Product Code IME
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5700
Decision Date 1979-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WARM-EE HEAT PACK received FDA 510(k) clearance under submission number K791684, sponsored by U.S. Export Marketing Group, 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 1979-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code IME and 21 CFR 890.5700, within the Physical Medicine review panel as a Class I device.