• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
258 records meeting your search criteria returned- Product Code: DQO Product Problem: Break Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR DRAGONFLY¿ OPTIS¿ IMAGING CATHETER 01/04/2024
ABBOTT VASCULAR DRAGONFLY OPSTAR IMAGING CATHETER 12/26/2023
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 11/28/2023
MICROVENTION, INC. HEADWAY-DUO 16 11/23/2023
TERUMO CORPORATION, ASHITAKA RADIFOCUS GLIDECATH HYDROPHILIC COATED C 11/21/2023
TERUMO MEDICAL CORPORATION RADIFOCUS GLIDECATH HYDROPHILIC COATED C 11/21/2023
TERUMO MEDICAL CORPORATION PROGREAT CATHETER 11/20/2023
ABBOTT VASCULAR DRAGONFLY¿ OPTIS¿ IMAGING CATHETER 10/27/2023
COOK INC TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETE 10/06/2023
MICROVENTION, INC. HEADWAY-DUO 16 10/02/2023
-
-