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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact