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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