Lumendi, LLC
FDA 510(k) & PMA Approved Dispositivos — 8 products
Publicidad
Total de dispositivos8
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K221452 | DiLumen C1, EZ1 and Tool Mount | FDF | 2023-02-10 | Ver |
| 510(k) | K211819 | DiLumen C2 and Tool Mount | FDF | 2021-10-22 | Ver |
| 510(k) | K210851 | DiLumen Endolumenal Interventional Platform (DiLumen) | FDF | 2021-04-21 | Ver |
| 510(k) | K183112 | DiLumen Endolumenal Interventional Knife (“DiLumen IK™”) | GEI | 2019-08-02 | Ver |
| 510(k) | K182540 | DiLumen Endolumenal Interventional Platform | FDF | 2018-10-30 | Ver |
| 510(k) | K173405 | DiLumen Endolumenal Interventional Scissors (DiLumen Is) | GEI | 2018-05-22 | Ver |
| 510(k) | K173317 | DiLumen C2; DiLumen Tool Mount | FDF | 2018-04-17 | Ver |
| 510(k) | K162428 | DiLumen Endolumenal Interventional Platform | FDF | 2016-12-06 | Ver |
No hay dispositivos coincidentes.