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FDA 510(k) Applications Submitted by ARKRAY FACTORY INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K142336
08/21/2014
GLUCOCARD 01 Blood Glocose Monitoring System/ReliOn Confirm Blood Glucose Monitoring System
ARKRAY FACTORY INC.
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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