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
 

 
 
 1 
 2 
 > 
 
13 records meeting your search criteria returned- Product Code: NRY Patient Problem: Reocclusion Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. PENUMBRA SYSTEM JET 7 REPERFUSION CATHET 10/11/2019
PENUMBRA, INC. PENUMBRA SYSTEM 5MAX ACE REPERFUSION CAT 04/28/2016
PENUMBRA, INC. PENUMBRA SYSTEM 4MAX REPERFUSION CATHETE 04/28/2016
CONCENTRIC MEDICAL TREVO PROVUE 09/24/2015
EV3 NEUROVASCULAR SOLITAIRE FR 08/14/2014
PENUMBRA, INC. PENUMBRA SYSTEM SEPARATOR 032 06/19/2014
PENUMBRA, INC. PENUMBRA SYSTEM 5MAX REPERFUSION CATHETE 06/19/2014
PENUMBRA, INC. PENUMBRA SYSTEM 5MAX SEPARATOR 06/19/2014
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX SEPARATOR 06/04/2014
PENUMBRA, INC. PENUMBRA SYSTEM REPERFUSION CATHETER 032 05/09/2014
-
-