• 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
 

 
 
5 records meeting your search criteria returned- Product Code: DWF Patient Problem: Arrhythmia Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ANGIODYNAMICS ANGIOVAC 02/12/2020
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANULA 10/29/2019
MAQUET CARDIOPULMONARY AG CATHETER, CANNULA AND TUBING VASCULAR 10/02/2018
COOK VASCULAR INC VITAL PORT DETACHED SILICONE CATHETER TI 03/04/2015
EDWARDS LIFESCIENCES PROPLEGE CORONARY SINUS CATHETER 07/03/2014
-
-