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INSTANT WARM GEL PACK

K912715 Class I Traditional
Decision Date
1991-10-02
Sponsor / Applicant
Prism Technologies, Inc.

Technical Specification

510(k) Submission ID K912715
Product Code IMD
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5710
Decision Date 1991-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTANT WARM GEL PACK received FDA 510(k) clearance under submission number K912715, sponsored by Prism Technologies, 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 1991-10-02.

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.