• 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 
 
 
30 records meeting your search criteria returned- Product Code: NIK Patient Problem: Myocardial Infarction Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) UNIFY QUADRA CRT-D, US MODEL, DF4COMP 11/23/2016
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) UNIFY ASSURA ICD 11/17/2016
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ASSURA CRT-D QUAD RF HV 10/27/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. VIVA QUAD XT 04/07/2016
MEDTRONIC DEFIBRILLATOR 11/02/2015
MEDTRONIC DEFIBRILLATOR 11/02/2015
BIOTRONIK SE & CO. KG LUMAX 540 HF-T 05/20/2015
GUIDANT CRM CLONMEL IRELAND DYNAGEN 09/04/2014
BIOTRONIK, INC. LUMAX 07/10/2014
CPI - DEL CARIBE EASYTRAK 2 01/13/2014
-
-