Ultromics Limited
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest FDA decision2024-11-15
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240860 | EchoGo Amyloidosis (1.0) | SDJ | 2024-11-15 | View |
| 510(k) | K240013 | EchoGo Heart Failure (2.0) | QUO | 2024-09-23 | View |
| 510(k) | K222463 | EchoGo Heart Failure | QUO | 2022-11-23 | View |
| 510(k) | K213275 | EchoGo Core (2.0) | QIH | 2021-12-20 | View |
No matching devices.