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FDA 510(k) Applications Submitted by RAYMOND BOULE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K071026
04/11/2007
BD GENEOHM STAPHSR ASSAY
BD DIAGNOSTICS (GENEOHM SCIENCES CANADA, INC)
K081920
07/03/2008
BD GENEOHM CDIFF ASSAY
BD DIAGNOSTICS (GENEOHM SCIENCES, INC.)
K102416
08/24/2010
BD GENEOHM VANR ASSAY
BD DIAGNOSTICS SCIENCE
K093346
10/26/2009
BD GENEOHM MRSA ACP ASSAY
BD DIAGNOSTICS (GENEOHM SCIENCES, INC.)
K120138
01/17/2012
BD MAX MRSA ASSAY, BD MAX INSTRUMENT
BD DIAGNOSTICS (GENEOHM SCIENCES CANADA, INC)
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