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 
 > 
 
20 records meeting your search criteria returned- Product Code: DRA Patient Problem: Vascular Dissection Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 01/19/2024
MEDTRONIC, INC. DEFLECTABLE SHEATH 01/03/2024
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER (CE) 08/14/2023
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 04/25/2023
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 03/08/2023
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 02/22/2023
ABBOTT MEDICAL MITRACLIP¿ G4 STEERABLE GUIDE CATHETER ( 01/10/2023
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 11/02/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 05/03/2022
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 03/23/2022
-
-