Abbott Vascular
FDA 510(k) & PMA Approved Produkte — 11 products
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Produkte insgesamt11
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Neueste FDA-Entscheidung
| Typ | Nummer | Produktname | Code | Datum | Aktionen |
|---|---|---|---|---|---|
| 510(k) | K220634 | NC TREK NEO Coronary Dilatation Catheter | LOX | 2022-06-30 | Anzeigen |
| 510(k) | K221057 | Viatrac 14 Plus Peripheral Dilatation Catheter | LIT | 2022-05-05 | Anzeigen |
| 510(k) | K201834 | HI-TORQUE PROCEED Guide Wire Family | DQX | 2020-07-30 | Anzeigen |
| 510(k) | K200144 | HI-TORQUE Steelcore Bare Guide Wire | DQX | 2020-04-08 | Anzeigen |
| 510(k) | K193126 | HI-TORQUE InfilTrac Guide Wire Family | DQX | 2019-12-11 | Anzeigen |
| 510(k) | K191173 | Emboshield NAV6 Embolic Protection System, Barewire Filter Delivery Wires | NTE | 2019-07-25 | Anzeigen |
| 510(k) | K180040 | NC TREK™ RX Coronary Dilatation Catheter; NC TREK™ OTW Coronary Dilatation Catheter; TREK™ RX Coronary Dilatation Catheter; TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ RX Coronary Dilatation Catheter; MINI TREK™ OTW Coronary Dilatation Catheter; MINI TREK™ II OTW Coronary Dilatation Catheter | LOX | 2018-08-24 | Anzeigen |
| 510(k) | K173795 | HI-TORQUE TurnTrac Guide Wire Family | DQX | 2018-01-12 | Anzeigen |
| 510(k) | K172394 | Steerable Guide Catheter | DRA | 2017-09-06 | Anzeigen |
| 510(k) | K172073 | Hi-Torque Command 18 Guide Wire | DQX | 2017-08-25 | Anzeigen |
| 510(k) | K161985 | Steerable Guide Catheter | DRA | 2016-08-07 | Anzeigen |
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