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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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