• 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
 

 
 
8 records meeting your search criteria returned- Product Code: DRA Patient Problem: Pulmonary Embolism Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 06/05/2023
ABBOTT MEDICAL G4 STEERABLE GUIDING CATHETER 05/08/2023
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 12/06/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 04/28/2022
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 06/11/2021
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 05/03/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 11/05/2020
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 03/23/2018
-
-