• 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: Noise, Audible Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR STEERABLE GUIDE CATHETER 08/09/2019
ABBOTT VASCULAR STEERABLE GUIDE CATHETER 08/07/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 06/18/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 05/16/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/12/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 02/14/2019
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 11/28/2018
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 09/11/2018
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 04/02/2018
AV-TEMECULA-CT MITRACLIP SYSTEM STEERABLE GUIDE CATHETE 02/02/2018
-
-