• 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 
 > 
 
28 records meeting your search criteria returned- Product Code: DQO Patient Problem: Embolism Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC, INC DXTERITY TRA 02/24/2020
MEDTRONIC, INC DXTERITY TRA 02/24/2020
ST. JUDE MEDICAL CATD DRAGONFLY¿ OPTIS¿ KIT BOX IMAGING CATHET 11/27/2019
ARGON MEDICAL DEVICES ARGON PICC CATH FIRST 26GA 1.9 FR 50 CM 01/29/2019
BOSTON SCIENTIFIC CORPORATION IMPULSE 10/12/2018
CORDIS CASHEL 466P306X 10/04/2018
CORDIS CORPORATION CATH F5.2ST+ JL 4 100CM 08/10/2018
CORDIS CASHEL 466P306X 07/18/2018
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER 06/15/2018
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 05/29/2018
-
-