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FDA 510(k) Applications Submitted by DENKA SEIKEN'S
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011400
05/07/2001
MRSA-SCREEN
DENKA SEIKEN'S
K981734
05/18/1998
VTEC-RPLA SEIKEN
DENKA SEIKEN'S
K011958
06/22/2001
CRP-LATEX (II) SEIKEN HIGH SENSITIVITY ASSAY KIT
DENKA SEIKEN'S
K013359
10/10/2001
LP(A)-LATEX SEIKEN ASSAY KIT
DENKA SEIKEN'S
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