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INSTANT COLD PACK

K963666 Class I Traditional
Decision Date
1996-10-30
Sponsor / Applicant
Kick Ice, Inc.

Technical Specification

510(k) Submission ID K963666
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1996-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTANT COLD PACK received FDA 510(k) clearance under submission number K963666, sponsored by Kick Ice, 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 1996-10-30.

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.