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FDA 510(k) Applications Submitted by Arkray Factory, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170064
01/09/2017
GLUCOCARD W Blood Glucose Monitoring System
ARKRAY FACTORY, INC.
K162822
10/07/2016
ADAMS A1c HA-8180V, CALIBRATOR 80
Arkray Factory, Inc.
K183306
11/28/2018
GLUCOCARD« W onyx Blood Glucose Monitoring System
ARKRAY Factory, Inc.
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