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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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