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
 

 
 
7 records meeting your search criteria returned- Product Code: QCA Patient Problem: Obstruction/Occlusion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROVENTION, INC. LVIS HDE 02/21/2024
MICROVENTION, INC. LVIS D 05/11/2023
MICROVENTION, INC. LVIS D 04/18/2023
MICROVENTION EUROPE LVIS EVO 2.5X17 MM 10/27/2022
MICROVENTION, INC. LVIS EVO 10/06/2022
MICROVENTION, INC. LVIS D 12/05/2020
MICROVENTION, INC. LVIS D 12/05/2020
-
-