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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
212 records meeting your search criteria returned- Product Code: DQO Product Problem: Detachment Of Device Component Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CORPORATION TEMPO 4 ANGIOGRAPHY CATHETER 08/18/2016
CORDIS CORPORATION TEMPO 4 ANGIOGRAPHY CATHETER 08/15/2016
BARD BARD PER-Q-CATH 08/11/2016
BOSTON SCIENTIFIC - MAPLE GROVE EXPO GUIDE CATHETER 08/09/2016
BOSTON SCIENTIFIC - FREMONT (SUD) ATLANTIS¿ SR PRO² 07/25/2016
CORDIS CORPORATION MULTIPACK ST+ F6 07/11/2016
BOSTON SCIENTIFIC - MAPLE GROVE IMAGER II ANGIOGRAPHIC CATHETER 07/05/2016
CORDIS CORPORATION FR5 INFINITI MULTIPAC 07/01/2016
BOSTON SCIENTIFIC - MAPLE GROVE IMAGER II ANGIOGRAPHIC CATHETER 06/29/2016
CORDIS CORPORATION CATH 5F INFINITI TL PIG145 110 06/28/2016
-
-