Geneohm Sciences Canada, Inc. (Bd Diagnostics)
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191957 | BD MAX Vaginal Panel | PQA | 2019-10-21 | View |
| 510(k) | K132822 | BD MAX STAPHSR ASSAY, INSTRUMENT | NQX | 2013-11-26 | View |
| 510(k) | K130470 | BD MAX CDIFF ASSAY, BD MAX INSTRUMENT | OZN | 2013-04-02 | View |
No matching devices.
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