• 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
192 records meeting your search criteria returned- Product Code: LWP Product Problem: Failure of Device to Self-Test Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC, INC. DUAL CHAMBER TEMPORARY PACEMAKER 05/17/2023
MEDTRONIC, INC. DUAL CHAMBER TEMPORARY PACEMAKER 08/17/2022
MEDTRONIC MILACA, INC. DUAL CHAMBER TEMPORARY PACEMAKER 04/13/2022
MEDTRONIC MILACA, INC. DUAL CHAMBER TEMPORARY PACEMAKER 11/18/2020
MEDTRONIC MILACA, INC. DUAL CHAMBER TEMPORARY PACEMAKER 09/02/2020
MEDTRONIC MILACA, INC. PULSE-GENERATOR, DUAL CHAMBER, IMPLANTAB 04/25/2018
MEDTRONIC MILACA, INC. PULSE-GENERATOR, DUAL CHAMBER, IMPLANTAB 04/10/2018
MEDTRONIC, INC. PULSE-GENERATOR, DUAL CHAMBER, IMPLANTAB 06/08/2017
MEDTRONIC, INC. PULSE-GENERATOR, DUAL CHAMBER, IMPLANTAB 12/09/2016
MEDTRONIC MILACA, INC. PULSE-GENERATOR, DUAL CHAMBER, IMPLANTAB 04/08/2016
-
-