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
 

 
 < 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 19 
 > 
 
193 records meeting your search criteria returned- Product Code: OUT Patient Problem: Therapeutic Response, Decreased Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
COVIDIEN (IRVINE) PIPELINE EMBOLIZATION DEVICE 08/09/2016
-
-