Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
23 records meeting your search criteria returned- Product Code: NIQ Product Problem: Unintended System Motion Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 11/20/2021
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 10/27/2021
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 10/20/2021
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 09/30/2021
ABBOTT VASCULAR XIENCE XPEDITION 48 EVEROLIMUS ELUTING C 04/15/2021
ABBOTT VASCULAR XIENCE XPEDITION 48 EVEROLIMUS ELUTING C 03/10/2021
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 03/05/2021
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 03/02/2021
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 03/02/2021
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 03/01/2021
-
-