Diality, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-12-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243607 | Moda-flx Hemodialysis System™ Cartridge (102121-001 ) | FJK | 2024-12-20 | View |
| 510(k) | K233798 | Moda-flx Hemodialysis System and Cartridge | KDI | 2024-08-02 | View |
No matching devices.