meddevicedb.com FDA Device Reference

HEAT PACK

K841698 Class I Traditional
Decision Date
1984-05-10
Sponsor / Applicant
Maddak, Inc.

Technical Specification

510(k) Submission ID K841698
Product Code IMA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5730
Decision Date 1984-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEAT PACK received FDA 510(k) clearance under submission number K841698, sponsored by Maddak, 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 1984-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code IMA and 21 CFR 890.5730, within the Physical Medicine review panel as a Class I device.