meddevicedb.com FDA Device Reference

INSULIN PROTECTOR

K073555 Class I Traditional
Decision Date
2008-07-11
Sponsor / Applicant
Medicool, Inc.

Technical Specification

510(k) Submission ID K073555
Product Code IQG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 2008-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSULIN PROTECTOR received FDA 510(k) clearance under submission number K073555, sponsored by Medicool, 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 2008-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code IQG and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.