• 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
 

 
 
 1 
 2 
 > 
 
19 records meeting your search criteria returned- Product Code: DQK Product Problem: Overheating of Device Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC CARTO® 3 SYSTEM 03/31/2024
BIOSENSE WEBSTER INC CARTO 3 SYSTEM 02/16/2024
BIOSENSE WEBSTER INC CARTO® 3 SYSTEM 01/10/2024
BIOSENSE WEBSTER INC CARTO 3 SYSTEM 05/31/2023
EATON CORPORATION TRIPPLITE POWER OUTLET, POWER TAP 04/20/2023
EDWARDS LIFESCIENCES HEMOSPHERE OXIMETRY CABLE 02/05/2019
BIOSENSE WEBSTER INC CARTO® 3 SYSTEM 07/12/2018
MERGE HEALTHCARE MERGE HEMODYNAMICS 05/07/2018
MERGE HEALTHCARE MERGE HEMODYNAMICS 01/11/2018
MERGE HEALTHCARE MERGE HEMODYNAMICS 12/12/2017
-
-