FDA 510(k) Applications Submitted by Kay Wu

FDA 510(k) Number	Submission Date	Device Name	Applicant
K170143	01/17/2017	GE Blood Glucose Monitoring System 180, GE Blood Glucose Monitoring System 182, Rightest Blood Glucose Monitoring System GM280, Rightest Blood Glucose Monitoring System GM280B,	Bionime Corporation
K173139	09/29/2017	Rightest Blood Glucose Monitoring System Wiz, Rightest Blood Glucose Monitoring System Wiz Plus	Bionime Corporation
K173638	11/24/2017	Rightest Blood Glucose Monitoring System Max, Rightest Blood Glucose Monitoring System Max Plus, GE Blood Glucose Monitoring System Max, GE Blood Glucose Monitoring System Max Plus	Bionime Corporation