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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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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
PHILIPS MEDICAL SYSTEMS SWITCHED INTERNAL PADDLES - 7.5 CM 07/17/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 07/17/2014
AGILENTTECHNOLOGIES, INC. CODEMASTER XL+ 07/16/2014
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 07/14/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 07/08/2014
ZOLL MEDICAL CORP PROPAQ MD DEFIBRILLATOR 07/03/2014
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 06/24/2014
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 06/19/2014
PHILIPS MEDICAL SYSTEMS SWITCHED INTERNAL PADDLES -4.5 CM 06/19/2014
PHILIPS MEDICAL SYSTEMS LARGE SWITCHLESS INTERNAL PADDLES 06/13/2014
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