Angeion Corp.
FDA 510(k) & PMA Approved Devices — 7 products
Advertisement
Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K921757 | ANGEION IGITAL ANGEFLATOR | MAV | 1993-03-18 | View |
| 510(k) | K925533 | ANGESTAT(R) PERICARDIAL DRAINAGE SHEATH SET | GBX | 1993-01-12 | View |
| 510(k) | K915719 | ANGEION ENDOSCOPIC VALVE SEAL | ODC | 1992-02-18 | View |
| 510(k) | K902377 | ANGEFLATOR(TM) | DXT | 1990-12-13 | View |
| 510(k) | K895580 | Y-ADAPTER W/THOUY BORST | DYB | 1990-04-30 | View |
| 510(k) | K894446 | ANGEION HEMOSTASIS VALVE INTRODUCER | DYB | 1989-11-30 | View |
| 510(k) | K871153 | CATHETER INTRODUCER | DYB | 1987-06-24 | View |
No matching devices.
Advertisement