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MEDISENSE PEN 2/COMPANION 2 BLOOD GLUCOSE SYSTEM

K901613 Class II Traditional
Decision Date
1990-07-10
Sponsor / Applicant
Medisense, Inc.

Technical Specification

510(k) Submission ID K901613
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1990-07-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDISENSE PEN 2/COMPANION 2 BLOOD GLUCOSE SYSTEM received FDA 510(k) clearance under submission number K901613, sponsored by Medisense, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1990-07-10.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.