Nipro Medical Corporation
FDA 510(k) & PMA Approved Dispositivos — 12 products
Publicidad
Total de dispositivos12
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K261399 | ELISIO™-HX | QAX | 2026-07-28 | Ver |
| 510(k) | K253047 | PRESSONE™ | FMI | 2026-03-24 | Ver |
| 510(k) | K260533 | ELISIO™-H | KDI | 2026-03-19 | Ver |
| 510(k) | K222852 | Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle | FMI | 2023-05-25 | Ver |
| 510(k) | K212677 | aboNT SYRINGE | FMF | 2022-04-15 | Ver |
| 510(k) | K190037 | Cronus HP PTA Balloon Catheter | LIT | 2019-10-24 | Ver |
| 510(k) | K191359 | Nipro Syringe | FMF | 2019-10-09 | Ver |
| 510(k) | K182940 | Surdial DX Hemodialysis System | KDI | 2019-07-19 | Ver |
| 510(k) | K173029 | Nipro Syringe | FMF | 2018-03-30 | Ver |
| 510(k) | K161681 | Nipro SafeTouch IV Catheter | FOZ | 2017-03-08 | Ver |
| 510(k) | K160444 | FB-U Hemodialyzer | KDI | 2017-02-08 | Ver |
| 510(k) | K151141 | Cronus HP - High Pressure Peripheral Balloon Catheter | LIT | 2016-01-14 | Ver |
No hay dispositivos coincidentes.