• 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 
 > 
 
21 records meeting your search criteria returned- Product Code: NIQ Product Problem: Difficult or Delayed Activation Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SIERRA 12/30/2019
ABBOTT VASCULAR XIENCE SIERRA 11/25/2019
ABBOTT VASCULAR XIENCE SIERRA 10/23/2019
ABBOTT VASCULAR XIENCE DRUG ELUTING CORONARY STENT 10/09/2019
ABBOTT VASCULAR XIENCE SIERRA 08/15/2019
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 06/28/2019
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 06/07/2019
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 05/02/2019
AV-TEMECULA-CT XIENCE PROX EVEROLIMUS ELUTING RX CORON 04/09/2019
AV-TEMECULA-CT XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 03/21/2019
-
-