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

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 
 > 
 
17 records meeting your search criteria returned- Product Code: DYB Patient Problem: Transient Ischemic Attack Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
W. L. GORE & ASSOCIATES, INC. GORE® DRYSEAL FLEX INTRODUCER SHEATH 06/24/2022
ST. JUDE MEDICAL SWARTZ¿ INTRODUCER, UNKNOWN 03/07/2022
ST. JUDE MEDICAL AGILIS¿ INTRODUCER, UNKNOWN 03/07/2022
BAYLIS MEDICAL COMPANY INC. TORFLEX TRANSSEPTAL GUIDING SHEATH 01/13/2022
ST. JUDE MEDICAL SWARTZ INTRODUCER, UNKNOWN 06/17/2021
ST. JUDE MEDICAL AGILIS INTRODUCER, UNKNOWN 06/17/2021
ST. JUDE MEDICAL AGILIS INTRODUCER, UNKNOWN 01/28/2021
ST. JUDE MEDICAL SWARTZ INTRODUCER, UNKNOWN 01/28/2021
ST. JUDE MEDICAL AGILIS INTRODUCER, UNKNOWN 10/07/2020
ST. JUDE MEDICAL, COSTA RICA LTDA AGILIS INTRODUCER, UNKNOWN 09/04/2020
-
-