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 
 3 
 > 
 
21 records meeting your search criteria returned- Product Code: DWF Patient Problem: Pulmonary Embolism Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 01/14/2022
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 03/19/2021
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 02/26/2021
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 11/03/2020
ANGIODYNAMICS ANGIOVAC 09/27/2019
MAQUET CARDIOPULMONARY AG CATHETER, CARDIOPULMONARY BYPASS 12/17/2018
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 06/26/2018
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 11/02/2017
ANGIODYNAMICS ANGIOVAC / ANGIODYNAMICS 01/10/2017
ANGIODYNAMICS ANGIODYNAMICS / ANGIOVAC 12/06/2016
-
-