FDA 510(k) Applications Submitted by PATRICIA DIONNE

FDA 510(k) Number Submission Date Device Name Applicant
K130470 02/25/2013 BD MAX CDIFF ASSAY, BD MAX INSTRUMENT GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
K132822 09/09/2013 BD MAX STAPHSR ASSAY, INSTRUMENT GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)
K133605 11/25/2013 BD MAX MRSA XT, BD MAX INSTRUMENT GENEOHM SCIENCES CANADA, INC.


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