Interson Corporation
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-12-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K233734 | Interson USB Ultrasound System | IYN | 2023-12-22 | View |
| 510(k) | K163443 | Interson USB Ultrasound System | IYN | 2017-04-13 | View |
No matching devices.