Siemens Healthineers
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-07-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K241898 | Symbia SPECT and SPECT/CT Systems | KPS | 2024-07-26 | View |
| 510(k) | K183575 | ACUSON S3000, S2000 Diagnostic Ultrasound System | IYN | 2019-03-20 | View |
No matching devices.