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 
 3 
 > 
 
26 records meeting your search criteria returned- Product Code: MCW Patient Problem: Obstruction/Occlusion Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND SILVERHAWK ATK 03/22/2024
COVIDIEN SILVERHAWK ATK 12/20/2023
BOSTON SCIENTIFIC CORPORATION JETSTREAM XC 11/16/2023
CARDIOVASCULAR SYSTEMS, INC. DIAMONDBACK 360 PERIPHERAL ORBITAL ATHER 11/03/2023
BOSTON SCIENTIFIC CORPORATION JETSTREAM XC 03/22/2023
BOSTON SCIENTIFIC CORPORATION JETSTREAM XC 12/08/2022
BOSTON SCIENTIFIC CORPORATION JETSTREAM SC 12/06/2022
UNKNOWN ROTAREX 09/07/2022
UNKNOWN ROTAREX 09/01/2022
MEDTRONIC IRELAND SILVERHAWK BTK 07/28/2022
-
-