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EUSURE BLOOD GLUCOSE MONITORING SYSTEM

K040678 Class II Traditional
Decision Date
2004-07-14
Sponsor / Applicant
Eumed Biotechnology Co., Ltd.

Technical Specification

510(k) Submission ID K040678
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2004-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EUSURE BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance under submission number K040678, sponsored by Eumed Biotechnology 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 2004-07-14.

Classification & Regulation

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