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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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