meddevicedb.com FDA Device Reference

HOT/COLD PACK HOLDERS

K823814 Class I Traditional
Decision Date
1983-01-14
Sponsor / Applicant
Danek Medical, Inc.

Technical Specification

510(k) Submission ID K823814
Product Code IME
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5700
Decision Date 1983-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOT/COLD PACK HOLDERS received FDA 510(k) clearance under submission number K823814, sponsored by Danek Medical, 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 1983-01-14.

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.