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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