Centervue S.P.A.
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories2
Latest FDA decision2025-03-17
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243504 | MAIA (AHMACME001) | MYC | 2025-03-17 | View |
| 510(k) | K234076 | iCare ALTIUS CW | NFJ | 2024-08-22 | View |
| 510(k) | K213705 | DRSplus | MYC | 2021-12-21 | View |
| 510(k) | K211328 | EIDON FA, EIDON, EIDON AF, EIDON UWFL | MYC | 2021-08-19 | View |
| 510(k) | K192113 | DRSplus | MYC | 2019-11-15 | View |
| 510(k) | K180526 | EIDON FA | MYC | 2018-07-16 | View |
| 510(k) | K180293 | Retia 2 | MYC | 2018-05-30 | View |
| 510(k) | K153181 | MAIA | MYC | 2016-06-08 | View |
No matching devices.