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

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 7 
 8 
 9 
 10 
 > 
 
162 records meeting your search criteria returned- Product Code: NIK Patient Problem: Heart Failure Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ASSURA ICD 10/25/2017
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUADRA ASSURA CRT-D QUAD RF HV 10/24/2017
GUIDANT CRM CLONMEL IRELAND INOGEN 10/24/2017
MEDTRONIC PUERTO RICO OPERATIONS CO. COMPIA MRI QUAD CRT-D 10/17/2017
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUADRA ASSURA MP ICD 10/13/2017
GUIDANT CRM CLONMEL IRELAND VIGILANT 10/10/2017
CPI - DEL CARIBE EASYTRAK 2 10/09/2017
CPI - DEL CARIBE EASYTRAK 3 10/09/2017
GUIDANT CRM CLONMEL IRELAND DYNAGEN 10/09/2017
MEDTRONIC PUERTO RICO OPERATIONS CO. VIVA QUAD XT 10/06/2017
-
-