Walk Vascular, LLC
FDA 510(k) & PMA Approved Dispositivos — 7 products
Publicidad
Total de dispositivos7
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K213565 | JETi AIO Peripheral Thrombectomy System | QEZ | 2022-02-01 | Ver |
| 510(k) | K201998 | JETi AIO Peripheral Thrombectomy System | QEZ | 2020-11-17 | Ver |
| 510(k) | K192439 | JETi Peripheral Thrombectomy System | QEZ | 2019-12-09 | Ver |
| 510(k) | K183403 | JETi 88 Peripheral Thrombectomy System | QEZ | 2019-04-17 | Ver |
| 510(k) | K172000 | ClearLumen II Peripheral Thrombectomy System | QEZ | 2017-10-24 | Ver |
| 510(k) | K163051 | ClearLumen II Peripheral Thrombectomy System | QEZ | 2017-02-21 | Ver |
| 510(k) | K161786 | ClearLumen II Thrombectomy System | QEZ | 2016-10-18 | Ver |
No hay dispositivos coincidentes.