• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
149 records meeting your search criteria returned- Product Code: NIQ Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE XPEDITION 10/14/2019
ABBOTT VASCULAR XIENCE SIERRA 10/08/2019
ABBOTT VASCULAR XIENCE SIERRA 10/08/2019
ABBOTT VASCULAR XIENCE XPEDITION 09/05/2019
ABBOTT VASCULAR XIENCE EVEROLIMUS ELUTING CORONARY STENT 09/04/2019
ABBOTT VASCULAR XIENCE PRIME EVEROLIMUS ELUTING CORONARY 09/04/2019
ABBOTT VASCULAR XIENCE ALPINE 08/02/2019
ABBOTT VASCULAR XIENCE SIERRA 07/26/2019
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 07/10/2019
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 07/09/2019
-
-