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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
133 records meeting your search criteria returned- Product Code: LPB Patient Problem: Cardiac Perforation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® BI-DIRECTIONAL 10/30/2022
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® UNI-DIRECTIONAL 10/28/2022
ST. JUDE MEDICAL SAFIRE¿ BI-DIRECTIONAL ABLATION CATHETER 10/18/2022
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH¿ ELECTROPHYSIOLO 10/10/2022
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 09/27/2022
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 09/19/2022
ST. JUDE MEDICAL LIVEWIRE¿ TC UNI-DIRECTIONAL ABLATION CA 09/06/2022
ST. JUDE MEDICAL LIVEWIRE¿ TC UNI-DIRECTIONAL ABLATION CA 09/06/2022
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 08/03/2022
BIOSENSE WEBSTER INC THERMOCOOL® SMART TOUCH® SF BI-DIRECTION 06/16/2022
-
-