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

Manufacturer and User Facility Device Experience (MAUDE)
  • 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 
 
 
50 records meeting your search criteria returned- Product Code: NRY Patient Problem: Perforation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. PENUMBRA SYSTEM 041 SEPARATOR 08/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM 041 REPERFUSION CATHETER 08/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM REPERFUSION CATHETER 041 05/01/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX SEPARATOR 03/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 03/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM 4MAX SEPARATOR 02/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM 4MAX REPERFUSION CATHETE 02/27/2014
PENUMBRA, INC. PENUMBRA SYSTEM SEPARATOR 054 01/16/2014
PENUMBRA, INC. PENUMBRA SYSTEM REPERFUSION CATHETER 054 01/16/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 01/09/2014
-
-