• 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 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
 
85 records meeting your search criteria returned- Product Code: NIM Product Problem: Premature Activation Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR XACT CAROTID STENT SYSTEM 12/27/2022
BOSTON SCIENTIFIC CORPORATION CAROTID WALLSTENT 12/08/2022
COVIDIEN PROTEGE RX CAROTID STENT SYSTEM 11/16/2022
ABBOTT VASCULAR XACT CAROTID STENT SYSTEM 10/12/2022
ABBOTT VASCULAR XACT CAROTID STENT SYSTEM 09/30/2022
ABBOTT VASCULAR RX ACCULINK CAROTID STENT SYSTEM 08/08/2022
BOSTON SCIENTIFIC CORPORATION CAROTID WALLSTENT 04/04/2022
CORDIS CASHEL PRECISE PRO RX US CAROTID SYST 02/28/2022
ABBOTT VASCULAR XACT CAROTID STENT SYSTEM 02/16/2022
COVIDIEN PROTEGE RX CAROTID STENT SYSTEM 09/06/2021
-
-