Roche Diabetes Care GmbH
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-08-10
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213134 | Accu-Chek Solo micropump system with interoperable technology | QFG | 2023-08-10 | View |
| 510(k) | K213131 | Accu-Chek Guide Solo diabetes manager blood glucose monitoring system | NBW | 2023-08-10 | View |
No matching devices.