• 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 
 4 
 5 
 6 
 7 
 > 
 
68 records meeting your search criteria returned- Product Code: NIQ Product Problem: Difficult or Delayed Activation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 10/23/2020
ABBOTT VASCULAR RX SIERRA 09/14/2020
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 06/03/2020
ABBOTT VASCULAR RX PRIME 04/08/2020
ABBOTT VASCULAR XIENCE XPEDITION 48 EVEROLIMUS ELUTING C 03/20/2020
ABBOTT VASCULAR XIENCE EVEROLIMUS ELUTING CORONARY STENT 03/19/2020
ABBOTT VASCULAR XIENCE SIERRA 03/13/2020
ABBOTT VASCULAR XIENCE SIERRA 12/30/2019
ABBOTT VASCULAR XIENCE SIERRA 11/25/2019
ABBOTT VASCULAR XIENCE SIERRA 10/23/2019
-
-