Aniara Diagnostica LLC
5 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| 5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905 recall (Z-2894-2026) | Aniara Diagnostica LLC | 2026-08-05 |
| 5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905 recall (Z-2895-2026) | Aniara Diagnostica LLC | 2026-08-05 |
| 5-PLASMA Bivalirudin Control, Model Number 5D-44905 recall (Z-2896-2026) | Aniara Diagnostica LLC | 2026-08-05 |
| ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A recall (Z-2171-2026) | Aniara Diagnostica LLC | 2026-05-12 |
| BIOPHEN Protein C 5 kit is for in vitro quantitative determination of Protein C activity o recall (Z-1227-2023) | Aniara Diagnostica LLC | 2023-03-06 |
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Every clearance here is in the API, with alerts when new ones post.