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FDA 510(k) Applications Submitted by MITSUBISHI KAGAKU IATRON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081360
05/15/2008
PATHFAST CK-MB-II, PATHFAST MYO-II
MITSUBISHI KAGAKU IATRON
K072189
08/06/2007
PATHFAST NTPROBNP AND D-DIMER TESTS
MITSUBISHI KAGAKU IATRON
K072288
08/16/2007
PATHFAST D-DIMER
MITSUBISHI KAGAKU IATRON
K083412
11/18/2008
PATHFAST HSCRP
MITSUBISHI KAGAKU IATRON
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