• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
474 records meeting your search criteria returned- Product Code: NIK Patient Problem: Device Overstimulation of Tissue Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION EASYTRAK 2 IS-1 01/14/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. CLARIA MRI QUAD CRT-D SURESCAN 11/11/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) UNIFY ASSURA ICD 02/07/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) UNIFY ASSURA CRT-D RF HV 11/15/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUADRA ASSURA CRT-D QUAD RF HV 09/05/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) UNIFY QUADRA CRT-D, US MODEL, DF4COMP 07/11/2018
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) UNIFY CRT-D 04/15/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUADRA ASSURA MP ICD 03/16/2018
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ASSURA ICD 03/07/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) UNIFY CRT-D 11/09/2017
-
-