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FDA 510(k) Applications Submitted by BD DIAGNOSTICS (GENEOHM SCIENCES, INC.)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K081920
07/03/2008
BD GENEOHM CDIFF ASSAY
BD DIAGNOSTICS (GENEOHM SCIENCES, INC.)
K093346
10/26/2009
BD GENEOHM MRSA ACP ASSAY
BD DIAGNOSTICS (GENEOHM SCIENCES, INC.)
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