• 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 
 3 
 
 
21 records meeting your search criteria returned- Product Code: MLV Patient Problem: Bradycardia Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL AMPLATZER PFO OCCLUDER 04/27/2023
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM ASD OCCLUDER 09/15/2022
ABBOTT MEDICAL AMPLATZER MULTI-FENESTRATED SEPTAL OCCLU 05/25/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 04/26/2022
ABBOTT MEDICAL AMPLATZER SEPTAL OCCLUDER 04/23/2022
ABBOTT MEDICAL AMPLATZER PFO OCCLUDER 02/04/2022
W. L. GORE & ASSOCIATES, INC. GORE CARDIOFORM ASD OCCLUDER 12/17/2020
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 12/13/2019
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 08/24/2017
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 04/05/2016
-
-