Leica Biosystems Imaging, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2026-08-07
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253554 | Aperio GT 450 DX; Aperio GT 180 DX | PSY | 2026-08-07 | View |
| 510(k) | K253561 | Aperio iQC DX Software | QKQ | 2026-08-07 | View |
| 510(k) | K232202 | Aperio GT 450 DX | PSY | 2024-04-16 | View |
| 510(k) | K190332 | Aperio AT2 DX System | PSY | 2019-05-20 | View |
No matching devices.