• 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 
 4 
 5 
 6 
 7 
 > 
 
68 records meeting your search criteria returned- Product Code: DRA Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 08/23/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 06/28/2022
CARDIOFOCUS HEARTLIGHT 02/18/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 01/11/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 11/08/2021
CARDIOFOCUS HEARTLIGHT 10/08/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 10/08/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 09/20/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 08/13/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 07/19/2021
-
-