• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: NTE Patient Problem: Thrombus Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN SPIDER FX 04/21/2020
SILK ROAD MEDICAL, INC ENROUTE NEUROPROTECTION SYSTEM 02/18/2020
INVATEC SPA MO.MA ULTRA 09/27/2019
SILK ROAD MEDICAL, INC. ENROUTE TRANSCAROTID NEUROPROTECTION SYS 07/26/2019
SILK ROAD MEDICAL, INC. ENROUTE TRANSCAROTID NEUROPROTECTION SYS 06/27/2019
SILK ROAD MEDICAL ENROUTE NEUROPROTECTION SYSTEM 05/22/2019
COVIDEN SPIDER FX 01/08/2019
COVIDIEN SPIDER FX 11/08/2018
INVATEC SPA MO.MA 10/26/2018
INVATEC SPA MO.MA ULTRA 07/13/2018
-
-