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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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118 records meeting your search criteria returned- Product Code: LDD Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 04/09/2014
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 04/02/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 03/27/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 03/20/2014
PHILIPS MEDICAL SYSTEMS SWITCHED INTERNAL PADDLES -4.5 CM 03/11/2014
PHYSIO-CONTROL LIFEPAK 12 03/06/2014
PHYSIO CONTROL LIFE PACK 12 03/05/2014
PHYSIO CONTROL LIFEPACK 12 DEFIBRILLATOR 03/05/2014
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 02/25/2014
PHYSIO-CONTROL, INC HANDLES AND CONNECTOR WITH DISCHARGE CON 02/18/2014
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