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INSTANT ICE PACK

K901834 Class I Traditional
Decision Date
1990-05-03
Sponsor / Applicant
Impact Packaging Corp.

Technical Specification

510(k) Submission ID K901834
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1990-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTANT ICE PACK received FDA 510(k) clearance under submission number K901834, sponsored by Impact Packaging Corp.. 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 1990-05-03.

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.