FDA 510(k) Applications Submitted by PHYSIO-CONTROL, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K182503 |
09/12/2018 |
Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors |
Physio-Control, Inc. |
K130454 |
02/22/2013 |
LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR |
PHYSIO-CONTROL, INC. |
K122600 |
08/27/2012 |
LIFEPAK 1000 DEFIBRILLATOR |
PHYSIO-CONTROL, INC. |
K102972 |
10/06/2010 |
LIFEPAK 12 |
PHYSIO-CONTROL, INC. |
K073089 |
11/01/2007 |
LIFEPAK 20E |
PHYSIO-CONTROL, INC. |
K103567 |
12/06/2010 |
LIFEPAK 15 MONITOR/DEFIBRILLATOR |
PHYSIO-CONTROL, INC. |
K142430 |
08/29/2014 |
LIFEPAK 15 monitor/defibrillator |
PHYSIO-CONTROL, INC. |
K102757 |
09/23/2010 |
LIFENET SYSTEM |
PHYSIO-CONTROL, INC. |
K082937 |
10/01/2008 |
LIFEPAK 15 MONITOR/DEFIBRILLATOR |
PHYSIO-CONTROL, INC. |
K123597 |
11/21/2012 |
TRUECPR COACHING DEVICE |
PHYSIO-CONTROL, INC. |
K093925 |
12/22/2009 |
LIFENET SYSTEM |
PHYSIO-CONTROL, INC. |
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