FDA 510(k) Applications Submitted by Bionime Coporation

FDA 510(k) Number Submission Date Device Name Applicant
K141292 05/19/2014 Rightest Blood Glucose Monitoring System GM700, Rightest Blood Glucose Monitoring System GM650, GE200 Blood Glucose Monitoring System, and GE300 Talking Blood Glucose Monitoring System BIONIME COPORATION
K133522 11/15/2013 RIGHTEST DIABETES MANAGEMENT SOFTWARE AND ADAPTER (EXISTING CLEARED K113007),RIGHTEST NEW ADAPTERS-3,GE DIABETES MANAGEM BIONIME COPORATION
K143387 11/26/2014 GE333 Blood Glucose Monitoring System Bionime Coporation


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