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Denka Seiken'S

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K011400 MRSA-SCREENMYI2002-03-27 View
510(k) K013359 LP(A)-LATEX SEIKEN ASSAY KITDFC2002-03-08 View
510(k) K011958 CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KITDCN2001-12-04 View
510(k) K981734 VTEC-RPLA SEIKENGNA1998-09-22 View
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