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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