• 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 
 > 
 
36 records meeting your search criteria returned- Product Code: NIQ Patient Problem: Cardiomyopathy Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC VASCULAR RESOLUTE ONYX STENT 02/10/2020
BOSTON SCIENTIFIC CORPORATION PROMUS PREMIER 09/05/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 11/01/2018
MEDTRONIC IRELAND RESOLUTE ONYX RX 08/13/2018
BOSTON SCIENTIFIC - GALWAY PROMUS ELEMENT¿ PLUS 10/11/2017
BOSTON SCIENTIFIC - GALWAY PROMUS ELEMENT¿ PLUS 10/07/2017
BOSTON SCIENTIFIC - GALWAY PROMUS ELEMENT¿ PLUS 10/07/2017
BOSTON SCIENTIFIC - GALWAY PROMUS ELEMENT¿ PLUS 10/07/2017
BOSTON SCIENTIFIC - GALWAY PROMUS ELEMENT¿ PLUS 09/26/2017
MEDTRONIC IRELAND RESOLUTE ONYX RX 06/29/2017
-
-