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BLOOD GLUCOSE MONITORING SYSTEM (GLUCOSE OXIDASE)

K113636 Class II Traditional
Decision Date
2013-03-08
Sponsor / Applicant
Philosys Co., Ltd.

Technical Specification

510(k) Submission ID K113636
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2013-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD GLUCOSE MONITORING SYSTEM (GLUCOSE OXIDASE) received FDA 510(k) clearance under submission number K113636, sponsored by Philosys Co., Ltd.. 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 2013-03-08.

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.