SENTINEL CH. SpA
FDA 510(k) & PMA Approved Devices — 11 products
Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K242585 | Cystatin C | NDY | 2025-05-16 | View |
| 510(k) | K211058 | Lp(a) Ultra | DFC | 2022-12-22 | View |
| 510(k) | K193001 | Albumin BCP | CJW | 2019-12-19 | View |
| 510(k) | K192118 | CRP Vario | DCK | 2019-11-08 | View |
| 510(k) | K173833 | CRP Vario | NQD | 2018-09-27 | View |
| 510(k) | K102706 | CKMB UDR ASSAY | JHS | 2011-08-19 | View |
| 510(k) | K083602 | KAPPA LIGHT CHAINS | DFH | 2009-09-03 | View |
| 510(k) | K083601 | LAMBDA LIGHT CHAINS | DEH | 2009-06-22 | View |
| 510(k) | K081533 | SENTINEL PLASMAPROTEINS CAL 3X | JIX | 2008-06-25 | View |
| 510(k) | K073634 | MULTIGENT CREATININE (ENZYMATIC) ASSAY | JFY | 2008-06-19 | View |
| 510(k) | K070987 | SENTINEL LITHIUM ASSAY | NDW | 2007-08-02 | View |
No matching devices.