Ocuject, 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) | K242956 | LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle | QNS | 2024-10-25 | Ver |
| 510(k) | K233343 | SteriCap Safety Needle; VitreJect Safety Needle | FMI | 2023-11-27 | Ver |
| 510(k) | K230959 | VitreJect® Needle; OcuSafe® Needle | FMI | 2023-09-14 | Ver |
| 510(k) | K230372 | VitreJect Syringe | QLY | 2023-09-08 | Ver |
| 510(k) | K212544 | MiniLoad Syringe | FMF | 2021-10-13 | Ver |
| 510(k) | K212805 | SteriCap Mini Needle and Standard Needles | FMI | 2021-09-30 | Ver |
| 510(k) | K202432 | MiniLoad Syringe | FMF | 2021-02-19 | Ver |
| 510(k) | K170768 | Mini Needle | FMI | 2017-07-10 | Ver |
No hay dispositivos coincidentes.