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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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117 records meeting your search criteria returned- Product Code: DRM Patient Problem: Cardiac Arrest Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 10/27/2014
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 10/10/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 09/16/2014
ZOLL CIRCULATION, INC AUTOPULSE® LI-ION BATTERY 09/04/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 09/04/2014
MICHIGAN INSTRUMENTS, INC. LIFE-STAT 09/02/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/13/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/04/2014
ZOLL CIRCULATION, INC AUTOPULSE® LI-ION BATTERY 08/04/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/04/2014
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