Sonavex, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2025-04-23
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243479 | EchoGuide (Version 1) | IYO | 2025-04-23 | View |
| 510(k) | K190039 | EchoSure Diagnostic Ultrasound System | IYO | 2019-03-08 | View |
| 510(k) | K180621 | EchoMark, EchoMark LP | NEU | 2018-06-06 | View |
No matching devices.