FDA 510(k) Applications Submitted by MICHELLE ACKERMANN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K130454 |
02/22/2013 |
LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR |
PHYSIO-CONTROL, INC. |
| K040775 |
03/26/2004 |
LIFEPAK 12 |
MEDTRONIC PHYSIO-CONTROL CORP. |
| K041459 |
06/02/2004 |
LIFEPAK 12 DEFIBRILLATOR/MONITOR |
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC. |
| K122600 |
08/27/2012 |
LIFEPAK 1000 DEFIBRILLATOR |
PHYSIO-CONTROL, INC. |
| K102972 |
10/06/2010 |
LIFEPAK 12 |
PHYSIO-CONTROL, INC. |
| K033275 |
10/10/2003 |
LIFEPAK 12, 20, 500, CR PLUS |
MEDTRONIC PHYSIO-CONTROL CORP. |
| K063119 |
10/12/2006 |
LIFEPAK 20 DEFIBRILLATOR/ MONITOR |
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC. |
| K073089 |
11/01/2007 |
LIFEPAK 20E |
PHYSIO-CONTROL, INC. |
| K063510 |
11/20/2006 |
LIFEPAK 12 DEFIBRILLATOR/MONITOR |
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC. |
| K103567 |
12/06/2010 |
LIFEPAK 15 MONITOR/DEFIBRILLATOR |
PHYSIO-CONTROL, INC. |
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