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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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460 records meeting your search criteria returned- Product Code: MKJ Product Problem: Inappropriate/Inadequate Shock/Stimulation Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK 15 DEFIBRILLATOR/MONITOR 01/16/2020
CARDIAC SCIENCE CORPORATION POWERHEART G5 AED AUTOMATIC 01/07/2020
PHILIPS MEDICAL SYSTEMS HEARTSTART MRX 01/07/2020
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK® 20E DEFIBRILLATOR/MONITOR 01/02/2020
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK® 20 DEFIBRILLATOR/MONITOR 12/27/2019
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK® 20 DEFIBRILLATOR/MONITOR 12/27/2019
PHILIPS MEDICAL SYSTEMS HEART START XL 12/26/2019
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 12/26/2019
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK(R) CR2 DEFIBRILLATOR 12/26/2019
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK® 1000 DEFIBRILLATOR 12/26/2019
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