Medtronic Physio-Control Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K040775 | LIFEPAK 12 | April 23, 2004 |
| K033275 | LIFEPAK 12, 20, 500, CR PLUS | November 6, 2003 |
| K022732 | INFANT/CHILD REDUCED ENERGY ELECTRODES | December 13, 2002 |
| K012274 | MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER | February 5, 2002 |
| K011144 | LIFEPAK 600 AUTOMATED EXTERNAL DEFIBRILLATOR | December 3, 2001 |
| K012428 | MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR | September 28, 2001 |
| K010918 | LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM | August 23, 2001 |
| K002445 | LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES | January 31, 2001 |