Medtronic Emergency Response Systems, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Advertisement
Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K063510 | LIFEPAK 12 DEFIBRILLATOR/MONITOR | MKJ | 2007-01-26 | View |
| 510(k) | K063119 | LIFEPAK 20 DEFIBRILLATOR/ MONITOR | MKJ | 2006-12-22 | View |
| 510(k) | K052057 | LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR | MKJ | 2006-02-17 | View |
| 510(k) | K052854 | LIFENET EXCHANGE SYSTEM | MSX | 2006-01-20 | View |
| 510(k) | K042404 | LIFEPAK, MODEL 1000 | MKJ | 2005-12-22 | View |
| 510(k) | K041459 | LIFEPAK 12 DEFIBRILLATOR/MONITOR | MKJ | 2004-07-01 | View |
No matching devices.
Advertisement