• 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 
 > 
 
24 records meeting your search criteria returned- Product Code: MAE Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER 06/05/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER II 05/28/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER 04/01/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER 03/24/2020
AGA MEDICAL CORPORATION AMPLATZER PICCOLO OCCLUDER 03/12/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER II 03/12/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER 02/12/2020
AGA MEDICAL CORPORATION AMPLATZER PICCOLO OCCLUDER 02/11/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER 02/03/2020
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER 01/20/2020
-
-