• 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 
 
 
28 records meeting your search criteria returned- Product Code: LWQ Product Problem: Backflow Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL PUERTO RICO, INC. SJM MECHANICAL HEART VALVE 03/25/2020
ST. JUDE MEDICAL PUERTO RICO, INC. SJM MECHANICAL HEART VALVE 03/25/2020
ST. JUDE MEDICAL PUERTO RICO, INC. SJM MECHANICAL HEART VALVE 03/25/2020
ST. JUDE MEDICAL PUERTO RICO, INC. SJM MECHANICAL HEART VALVE 03/20/2020
MEDTRONIC, INC. OPEN PIVOT STANDARD AORTIC HEART VALVE 02/28/2020
ST. JUDE MEDICAL CATD SJM MECHANICAL HEART VALVE (UNKNOWN) 01/02/2020
ST. JUDE MEDICAL CATD SJM REGENT HEART VALVE W/FLEX CUFF 11/26/2019
ST. JUDE MEDICAL PUERTO RICO, INC. SJM REGENT HEART VALVE W/FLEX CUFF 10/11/2019
-
-