• 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 
 
 
88 records meeting your search criteria returned- Product Code: NIQ Patient Problem: Hypersensitivity/Allergic reaction Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 07/10/2017
AV-TEMECULA-CT XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 07/10/2017
AV-TEMECULA-CT XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 07/10/2017
AV-TEMECULA-CT XIENCE V EVEROLIMUS ELUTING CORONARY STE 06/29/2017
AV-TEMECULA-CT XIENCE V EVEROLIMUS ELUTING CORONARY STE 06/29/2017
AV-TEMECULA-CT XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 02/06/2017
AV-TEMECULA-CT XIENCE XPEDITION EVEROLIMUS ELUTING CORO 01/09/2017
AV-TEMECULA-CT XIENCE XPEDITION EVEROLIMUS ELUTING CORO 01/09/2017
-
-