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CERTI COOL INSTANT COLD COMPRESS

K960624 Class I Traditional
Decision Date
1996-05-06
Sponsor / Applicant
Certified Safety Mfg., Inc.

Technical Specification

510(k) Submission ID K960624
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1996-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CERTI COOL INSTANT COLD COMPRESS received FDA 510(k) clearance under submission number K960624, sponsored by Certified Safety Mfg., 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 1996-05-06.

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.