• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: DQK Patient Problem: Arrhythmia Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL EP-4¿ CARDIAC STIMULATOR AND TOUCHSCREEN 02/28/2024
ST. JUDE MEDICAL EP-4¿ CARDIAC STIMULATOR AND TOUCHSCREEN 02/18/2024
ST. JUDE MEDICAL EP-4¿ CARDIAC STIMULATOR 08/21/2023
BIOSENSE WEBSTER INC CARTO 3 SYSTEM 02/24/2023
BIOSENSE WEBSTER INC CARTO® 3 SYSTEM 11/17/2022
ST. JUDE MEDICAL, INC. EP-4¿ 05/10/2022
ST. JUDE MEDICAL EP-WORKMATE AND WORKMATE CLARIS EP-4 TOU 09/23/2021
ST. JUDE MEDICAL, INC. WORKMATE CLARIS SYSTEM AMPLIFIER 05/18/2020
ST. JUDE MEDICAL, INC EP-WORKMATE¿ COMPUTER (HP Z600) 04/25/2018
ST. JUDE MEDICAL, INC. EP-WORKMATE¿ EP-4¿ CARDIAC STIMULATOR, 4 04/26/2017
-
-