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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