Sectra AB
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-04-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232208 | Sectra Digital Pathology Module (Version 3.3) | PSY | 2024-04-16 | View |
| 510(k) | K193054 | Sectra Digital Pathology Module | QKQ | 2020-03-31 | View |
No matching devices.