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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