Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
44 records meeting your search criteria returned- Product Code: NVZ Product Problem: No Apparent Adverse Event Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FORTIFY ASSURA DR ICD, US 04/08/2024
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ASSURITY RF DR 02/19/2024
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ASSURITY MRI 01/10/2024
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FORTIFY ASSURA DR ICD, US 01/05/2024
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FORTIFY VR, U1.6 SJ4 US 11/28/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FORTIFY VR, U1.6 SJ4 US 11/27/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ENDURITY DR 10/27/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FORTIFY VR, U1.6 SJ4 US 08/16/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ELLIPSE DR 08/14/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FORTIFY ASSURA DR ICD, US 06/20/2023
-
-