FDA 510(k) Applications Submitted by DIAMOND DIAGNOSTICS, INC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K120591 |
02/28/2012 |
DIAMOND TOKYO BOEKI ISE MODULE CALIBRATOR 1,2,1-2 |
DIAMOND DIAGNOSTICS, INC |
K121027 |
04/04/2012 |
DIAMOND CALIBRATOR LOW, DIAMOND CALIBRATOR HIGH |
DIAMOND DIAGNOSTICS, INC |
K121140 |
04/16/2012 |
PROLYTE ELECTROLYTE ANALYZER |
DIAMOND DIAGNOSTICS, INC |
K133751 |
12/09/2013 |
DIAMOND DIAGNOSTICS ISE SERUM STANDARDS, DIAMOND DIAGNOSTICS ISE URINE STANDARDS |
DIAMOND DIAGNOSTICS, INC |
K103364 |
11/16/2010 |
MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS, LEVEL 1, LEVEL 2, DUAL LEVEL |
DIAMOND DIAGNOSTICS, INC |
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