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

Manufacturer and User Facility Device Experience (MAUDE)
  • 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
244 records meeting your search criteria returned- Product Code: DRA Patient Problem: Air Embolism Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC DE COSTA RICA S.R.L. POLARSHEATH 04/06/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 03/23/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 02/02/2021
BOSTON SCIENTIFIC DE COSTA RICA S.R.L. POLARSHEATH 01/27/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 01/26/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 01/04/2021
CARDIOFOCUS HEARTLIGHT 12/17/2020
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 11/23/2020
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 11/18/2020
MEDTRONIC CRYOCATH LP FLEXCATH ADVANCE STEERABLE SHEATH 11/17/2020
-
-