FDA 510(k) Applications Submitted by MARI A MEYER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K131037	04/15/2013	LIAISON XL HCG	DIASORIN, INC.
K141116	04/30/2014	LIAISON XL ANALYZER	DIASORIN, INC.
K061820	06/28/2006	DIASORIN LIAISON VZV IGG	DIASORIN, INC.
K121944	07/03/2012	LIAISON DIRECT RENIN LIAISON CONTROL DIRECT RENIN LIAISON ENDOCRINOLOGY DILUENT	DIASORIN, INC.
K132492	08/09/2013	LIAISON 25 TOTAL-D	DIASORIN, INC.
K103529	12/01/2010	LIAISON XL ANALYZER MODEL 10050	DIASORIN, INC.
K073390	12/03/2007	DIASORIN LIASON RUBELLA IGG ASSAY; DIASORIN LIAISON RUBELLA IGG TRI-CONTROLS	DIASORIN, INC.
K052499	09/13/2005	DIASORIN LIAISON TOXO IGG AND LIAISON TOXO IGM ASSAYS	DIASORIN S.P.A.