• 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
 

 
 
5 records meeting your search criteria returned- Product Code: NJE Patient Problem: Hemorrhage, Intraventricular Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CODMAN AND SHURTLEFF, INC ENTERPRISE VASCULAR RECONSTRUCTION DEVIC 02/25/2016
STRYKER NEUROVASCULAR-CALIF NEUROFORM 3 - 4.0 X 30MM 10/29/2015
STRYKER NEUROVASCULAR-CALIF F/G WINGSPAN STENT SYSTEM 4.5 X 20MM 10/29/2015
STRYKER NEUROVASCULAR-CALIF F/G WINGSPAN STENT SYSTEM 4.5 X 20MM 02/06/2015
CODMAN ENTERPRISE STENT 12/09/2014
-
-