FDA 510(k) Applications Submitted by LIANN VOO

FDA 510(k) Number Submission Date Device Name Applicant
K082462 08/27/2008 GEMLYTE ELECTROLYTE ANALYZER NA+/K+/CL-/CA++/LI+ DIAMOND DIAGNOSTICS, INC.
K102959 10/05/2010 PROLYTE ELECTROLYTE ANALYZER 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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