• 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
 

 
 
8 records meeting your search criteria returned- Product Code: DRA Product Problem: Signal Artifact/Noise Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC. LIVEWIRE¿ ELECTROPHYSIOLOGY CATHETER DEC 10/27/2023
ST. JUDE MEDICAL, INC. LIVEWIRE¿ ELECTROPHYSIOLOGY CATHETER DEC 06/21/2023
ST. JUDE MEDICAL, INC. LIVEWIRE¿ ELECTROPHYSIOLOGY CATHETER DEC 06/21/2023
ST. JUDE MEDICAL, INC. LIVEWIRE¿ STEERABLE ELECTROPHYSIOLOGY CA 06/07/2023
ST. JUDE MEDICAL, INC. LIVEWIRE¿ STEERABLE ELECTROPHYSIOLOGY CA 06/06/2023
ST. JUDE MEDICAL, INC. LIVEWIRE¿ ELECTROPHYSIOLOGY CATHETER DEC 05/06/2022
ST. JUDE MEDICAL LIVEWIRE STEERABLE ELECTROPHYSIOLOGY CA 02/10/2021
ST. JUDE MEDICAL LIVEWIRE ELECTROPHYSIOLOGY CATHETER DECA 01/28/2021
-
-