• 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 
 > 
 
20 records meeting your search criteria returned- Product Code: DRA Product Problem: Physical Resistance/Sticking Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER (CE) 03/25/2024
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER (CE) 03/01/2024
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER (CE) 04/17/2023
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 03/09/2023
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 03/09/2023
SJM / ABBOTT MEDICAL LIVEWIRE STEERABLE ELECTROPHYSIOLOGY CAT 10/25/2022
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 09/15/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 03/24/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 03/10/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 01/31/2022
-
-