Medtronic Vascular, Inc.
FDA 510(k) & PMA Approved Dispositivos — 5 products
Publicidad
Total de dispositivos5
Categorías0
Última decisión de la FDA
| Tipo | Número | Nombre del dispositivo | Código | Fecha | Acciones |
|---|---|---|---|---|---|
| 510(k) | K182957 | Heli-FX EndoAnchor System | OTD | 2018-11-21 | Ver |
| 510(k) | K171866 | Sentrant Introducer Sheath with Hydrophilic Coating | DYB | 2017-12-20 | Ver |
| 510(k) | K170191 | SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System | MCW | 2017-06-16 | Ver |
| 510(k) | K171427 | Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor Cassette | OTD | 2017-06-13 | Ver |
| 510(k) | K161361 | HawkOne Directional Atherectomy System | MCW | 2016-10-14 | Ver |
No hay dispositivos coincidentes.