Phoenix Imaging
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K883845 | RESUBMITTED AI 5200 ULTRASOUND TRANSDUCER | DXK | 1989-02-03 | View |
| 510(k) | K880839 | AI 5200 DIAGNOSTIC ULTRASOUND SYSTEM | IYO | 1988-06-10 | View |
No matching devices.
Advertisement