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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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127 records meeting your search criteria returned- Product Code: DRM Product Problem: Device Stops Intermittently Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/21/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 08/18/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 06/23/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 05/28/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 05/27/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 05/22/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 02/11/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 12/11/2014
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 12/09/2014
MICHIGAN INSTRUMENTS, INC. LIFESTAT 09/02/2014
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