meddevicedb.com FDA Device Reference

MEG-2B Blood Glucose Monitoring System, MEG-2B Pro Blood Glucose Monitoring System

K143750 Class II Special
Decision Date
2015-05-07
Sponsor / Applicant
Apex BioTechnology Corp.

Technical Specification

510(k) Submission ID K143750
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2015-05-07
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEG-2B Blood Glucose Monitoring System, MEG-2B Pro Blood Glucose Monitoring System received FDA 510(k) clearance under submission number K143750, sponsored by Apex BioTechnology Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2015-05-07.

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.