• 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 
 > 
 
68 records meeting your search criteria returned- Product Code: OUT Patient Problem: Stenosis Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE 07/27/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE FLEX 07/24/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE FLEX EMBOLIZATION DEVICE 07/13/2020
STRYKER NEUROVASCULAR CORK UNKNOWN_NEUROVASCULAR_PRODUCT 07/01/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE FLEX 06/30/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE 06/08/2020
STRYKER NEUROVASCULAR CORK SURPASS STREAMLINE 3.0MM X 25MM - CE 04/28/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE 04/06/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE FLEX EMBOLIZATION DEVICE 04/06/2020
MICRO THERAPEUTICS, INC. DBA EV3 PIPELINE FLEX EMBOLIZATION DEVICE 04/05/2020
-
-