Biomérieux, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260619 | VITEK 2 AST-Streptococcus Cefepime (<=0.06 – >=4 µg/mL) | LON | 2026-09-28 | View |
| 510(k) | K212849 | VITEK 2 AST-Gram Positive Linezolid (<=0.5 – >=8 µg/mL) | LON | 2022-02-04 | View |
No matching devices.
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