• 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 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
147 records meeting your search criteria returned- Product Code: NIQ Patient Problem: Perforation of Vessels Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 03/07/2024
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 02/15/2024
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 02/13/2024
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 12/20/2023
BOSTON SCIENTIFIC CORPORATION PROMUS PREMIER 12/04/2023
BOSTON SCIENTIFIC CORPORATION PROMUS PREMIER 12/04/2023
BOSTON SCIENTIFIC CORPORATION PROMUS PREMIER 12/04/2023
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 12/03/2023
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 11/14/2023
ABBOTT VASCULAR XIENCE EVEROLIMUS ELUTING CORONARY STENT 10/03/2023
-
-