• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: NRY Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IRVINE SOLITAIRE FR2 02/04/2015
COVIDIEN SOLITAIRE FR 12/15/2014
PENUMBRA, INC. PENUMBRA SYSTEM 041 REPERFUSION CATHETER 08/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 08/22/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 08/12/2014
PENUMBRA, INC. PENUMBRA SYSTEM 5MAX ACE REPERFUSION CAT 06/19/2014
PENUMBRA, INC. PENUMBRA SYSTEM 5MAX ACE REPERFUSION CAT 06/19/2014
PENUMBRA, INC. PENUMBRA SYSTEM REPERFUSION CATHETER 041 05/01/2014
PENUMBRA, INC. PENUMBRA SYSTEM SEPARATOR 041 04/09/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 02/27/2014
-
-