• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
 
54 records meeting your search criteria returned- Product Code: MKJ Product Problem: Inaccurate Synchronization Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR 08/06/2019
PHYSIO-CONTROL, INC. - 3015876 LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR 06/21/2019
PHILIPS MEDICAL SYSTEMS HEART START XL 06/11/2019
ZOLL MEDICAL CORPORATION X SERIES 05/06/2019
PHILIPS MEDICAL SYSTEMS HEART START XL 03/06/2019
PHILIPS MEDICAL SYSTEMS HEARTSTART XL+ DEFIBRILLATOR/MONITOR 11/03/2018
PHILIPS MEDICAL SYSTEMS HEART START XL 10/10/2018
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 06/28/2018
PHYSIO-CONTROL, INC LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR 11/21/2017
ZOLL MEDICAL CORPORATION M SERIES 10/31/2017
-
-