• 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
 

 
 
9 records meeting your search criteria returned- Product Code: OJX Product Problem: Defibrillation/Stimulation Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
ST. JUDE MEDICAL DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
ST. JUDE MEDICAL DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
MEDTRONIC DRUG ELUTING PERMANENT LEFT VENTRICULAR 08/12/2023
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUARTET 11/10/2017
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX MICRO LV LEAD 07/05/2017
-
-