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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
332 records meeting your search criteria returned- Product Code: LWP Product Problem: Premature Elective Replacement Indicator Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ACCENT DR RF PACEMAKER 01/04/2019
ST. JUDE MEDICAL, INC. ACCENT DR 12/28/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ACCENT DR RF PACEMAKER 12/26/2018
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) ZEPHYR DR 12/21/2018
ST. JUDE MEDICAL, INC. ACCENT DR 12/18/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ZEPHYR DR 11/07/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ACCENT DR 11/05/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ZEPHYR XL DR 10/30/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) 5356 VERITY DR, AB 20 55 184 10/25/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) ACCENT SR 10/02/2018
-
-