Endocardial Solutions, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042493 | ENSITE SYSTEM, MODEL EE3000 | DQK | 2004-10-15 | View |
| 510(k) | K033211 | ENSITE SYSTEM | DQK | 2003-10-30 | View |
| 510(k) | K030129 | MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000 | DQK | 2003-04-22 | View |
| 510(k) | K012926 | MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000 | MTD | 2001-09-28 | View |
| 510(k) | K001437 | ENSITE 3000 SYSTEM, MODEL EE3000 | DQK | 2000-06-07 | View |
| 510(k) | K993376 | ENSTYLET MODELS EC0010, EC0020 | DRB | 2000-01-05 | View |
| 510(k) | K992479 | ENSITE 3000 SYSTEM | DQK | 1999-12-02 | View |
| 510(k) | K983456 | ENSITE 3000 SYSTEM | MTD | 1999-04-21 | View |
No matching devices.
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