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EVOLUTION BLOOD GLUCOSE MONITORING SYSTEM

K072369 Class II Traditional
Decision Date
2008-03-21
Sponsor / Applicant
Hmd Biomedical, LLC

Technical Specification

510(k) Submission ID K072369
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2008-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVOLUTION BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance under submission number K072369, sponsored by Hmd Biomedical, LLC. 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 2008-03-21.

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.