FDA 510(k) Applications Submitted by GENEOHM SCIENCES CANADA , INC (BD DIAGNOSTICS)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| DEN160001 | 01/11/2016 | BD MAX Vaginal Panel, BD MAX Instrument | GENEOHM SCIENCES CANADA , INC (BD DIAGNOSTICS) |
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