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
 

 
 
6 records meeting your search criteria returned- Product Code: DQX Patient Problem: Not Applicable Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC HEART VALVES DIVISION CONFIDA BRECKER CURVE GUIDEWIRE 12/21/2018
CORDIS CORPORATION DGW .035 FC J3MM 150CM TEF 12/14/2018
CORDIS CORPORATION SGW ATW .014 STR FLOPPY 195CM 11/09/2018
CORDIS CORPORATION CORDIS REFLEX STEERABLE GUIDEWIRE 07/15/2016
CORDIS CORPORATION CORDIS REFLEX STEERABLE GUIDEWIRE 07/15/2016
CORDIS CORPORATION CORDIS REFLEX STEERABLE GUIDEWIRE 07/15/2016
-
-