Zhejiang Curaway Medical Technology Co., Ltd.
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) | K260517 | Automatic Core Biopsy Instrument | KNW | 2026-08-28 | Ver |
| 510(k) | K244018 | Disposable Biopsy Needle | KNW | 2025-07-22 | Ver |
| 510(k) | K242322 | Bone Marrow Biopsy Needle | KNW | 2025-01-24 | Ver |
| 510(k) | K241793 | Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle | KNW | 2025-01-24 | Ver |
| 510(k) | K240758 | Radiofrequency Generator System, Cura RF Electrode | GEI | 2024-12-11 | Ver |
| 510(k) | K232505 | Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter | GEI | 2024-05-30 | Ver |
| 510(k) | K222001 | Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe | OAB | 2023-06-08 | Ver |
No hay dispositivos coincidentes.