Biosense, Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
Advertisement
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K961903 | MAGELLAN | HAW | 1998-08-24 | View |
| 510(k) | K960542 | NOGA | DRF | 1996-04-15 | View |
| 510(k) | K954395 | CARTO SYSTEM | DQK | 1995-12-21 | View |
No matching devices.
Advertisement