FDA 510(k) Applications Submitted by RAYMOND J 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)