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

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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
168 records meeting your search criteria returned- Product Code: OJX Product Problem: Signal Artifact/Noise Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT QUICKFLEX MICRO LV LEAD 10/18/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUARTET 10/03/2019
ABBOTT QUARTET 09/20/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUARTET 09/03/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUICKFLEX MICRO LV LEAD 07/12/2019
ABBOTT QUICKFLEX MICRO LV LEAD 07/11/2019
ABBOTT QUICKFLEX MICRO LV LEAD 07/08/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUARTET 07/03/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX XL LV LEAD 06/10/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUICKFLEX LV LEAD 06/05/2019
-
-