FDA 510(k) Applications Submitted by LONNA M DENDOOVEN

FDA 510(k) Number Submission Date Device Name Applicant
K142035 07/28/2014 GLUCOCARD 01-MINI BLOOD GLUCOSE MONITORING SYSTEM, RELION MICRO BLOOD GLUCOSE MONITORING SYSTEM ARKRAY FACTORY INC.
K124021 12/27/2012 ARKRAY GLUCOCARD 01 BLOOD GLUCOSE MONITORING SYSTEM AND RELION CONFIRM BLOOD GLUCOSE MONITORING SYSTEM ARKRAY FACTORY INC.


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