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FDA 510(k) Applications Submitted by Mari 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.
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