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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K011144
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The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 320217... 2 04/10/2013 Physio Control, Inc.
Medtronic Physio-Control LIFEPAK CR Plus Defibrillator/Monitor. Automated external defibrillator ... 1 09/14/2009 Physio Control, Inc.
LIFEPAK CR Plus Automated External Defibrillator (AED). Labeling on the device states LIFEPAK CR Pl... 2 10/30/2008 Physio Control, Inc.
LIFEPAK Express Automated External Defibrillator (AED). Labeling on the device states LIFEPAK CR Pl... 2 10/30/2008 Physio Control, Inc.
LIFEPAK CR Plus Automated External Defibrillator. Device is primarily deployed in Public Access Defi... 1 09/16/2008 Physio Control, Inc.
LIFEPAK CR Plus defibrillator 2 06/21/2007 Medtronic Emergency Response Systems, Inc.
LIFEPAK EXPRESS defibrillator 2 06/21/2007 Medtronic Emergency Response Systems, Inc.
LIFEPAK CR Plus defibrillator. The device is a battery operated, portable automated external defibr... 2 03/29/2007 Medtronic Emergency Response Systems, Inc.
LIFEPAK CR Plus defibrillator 2 06/12/2003 Medtronic Physio Control Corp
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