Raysolution Healthcare Co., Ltd.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2025-01-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K241266 | Imaging system of positron emission and X-ray computed tomography (DigitMI 930) | KPS | 2025-01-27 | View |
No matching devices.