• 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 
 > 
 
26 records meeting your search criteria returned- Product Code: DRA Patient Problem: Insufficient Information Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC DE COSTA RICA S.R.L. POLARSHEATH 06/17/2021
BOSTON SCIENTIFIC DE COSTA RICA S.R.L. POLARSHEATH 06/01/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/26/2021
BOSTON SCIENTIFIC DE COSTA RICA S.R.L. POLARSHEATH 04/22/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 04/15/2021
ABBOTT VASCULAR MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/13/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 04/09/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 04/07/2021
ABBOTT VASCULAR G4 STEERABLE GUIDING CATHETER 04/05/2021
BOSTON SCIENTIFIC DE COSTA RICA S.R.L. POLARSHEATH 04/02/2021
-
-