Selux Diagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest Approval2025-03-28
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K244044 | PBC Separator with Selux AST System | QZX | 2025-03-28 | View |
| 510(k) | K223493 | PBC Separator with Selux AST System | QZX | 2024-02-15 | View |
| 510(k) | K211748 | Selux AST System; Model AST Gen 1.0 | LON | 2023-04-19 | View |
| 510(k) | K211759 | Selux AST System; Model AST Gen 1.0 | LON | 2023-01-18 | View |
No matching devices.