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FDA 510(k) Applications Submitted by BD DIAGNOSTICS (GENEOHM SCIENCES CANADA, INC)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071026
04/11/2007
BD GENEOHM STAPHSR ASSAY
BD DIAGNOSTICS (GENEOHM SCIENCES CANADA, INC)
K120138
01/17/2012
BD MAX MRSA ASSAY, BD MAX INSTRUMENT
BD DIAGNOSTICS (GENEOHM SCIENCES CANADA, INC)
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