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
 

 
 
 1 
 2 
 3 
 > 
 
29 records meeting your search criteria returned- Product Code: MGB Product Problem: Occlusion Within Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AV-TEMECULA-CT PERCLOSE PROGLIDE 6F SUTURE MEDIATED CL 03/07/2018
AV-TEMECULA-CT PERCLOSE PROGLIDE 6F SUTURE MEDIATED CL 02/24/2018
TERUMO MEDICAL CORPORATION 6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVIC 09/26/2017
TERUMO ANGIO-SEAL VASCULAR CLOSURE DEVICE 06/13/2017
ABBOTT VASCULAR PERCLOSE PROGLIDE SUTURE-MEDIATED CLOSUR 05/05/2017
CARDIVA MEDICAL, INC. CARDIVA VASCADE 6/7F VCS 11/17/2016
CARDIVA MEDICAL, INC. CARDIVA VASCADE 5F VCS 11/17/2016
ABBOTT VASCULAR PERCLOSE 08/02/2016
ST. JUDE MEDICAL 6FR ANGIO SEAL 07/06/2016
ST. JUDE MEDICAL PUERTO RICO, B.V. ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEV 12/21/2015
-
-