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
 

 
 
8 records meeting your search criteria returned- Product Code: OAD Product Problem: Device Contamination with Body Fluid Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL FLEXABILITY¿ ABLATION CATHETER, SENSOR E 03/12/2024
BIOSENSE WEBSTER INC NAVISTAR® RMT THERMOCOOL® ELECTROPHYSIOL 11/11/2022
BIOSENSE WEBSTER INC NAVISTAR RMT THERMOCOOL ELECTROPHYSIOLOG 03/30/2021
BIOSENSE WEBSTER INC NAVISTAR DS ELECTROPHYSIOLOGY CATHETER 02/24/2021
BOSTON SCIENTIFIC CORPORATION INTELLANAV MIFI OPEN-IRRIGATED ABLATION 02/03/2021
BOSTON SCIENTIFIC CORPORATION INTELLANAV MIFI OPEN-IRRIGATED 09/22/2020
BIOSENSE WEBSTER, INC. (JUAREZ) THERMOCOOL® SMARTTOUCH® SF BI-DIRECTIONA 07/27/2016
BIOSENSE WEBSTER, INC (IRWINDALE) NAVISTAR® RMT THERMOCOOL® ELECTROPHYSIOL 01/22/2015
-
-