meddevicedb.com FDA Device Reference

THERMOELASTOMER HOT/COLD COMPRESS-7187-

K823650 Class I Traditional
Decision Date
1983-01-21
Sponsor / Applicant
Fred Sammons, Inc.

Technical Specification

510(k) Submission ID K823650
Product Code IME
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5700
Decision Date 1983-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERMOELASTOMER HOT/COLD COMPRESS-7187- received FDA 510(k) clearance under submission number K823650, sponsored by Fred Sammons, 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 1983-01-21.

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.