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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
110 records meeting your search criteria returned- Product Code: QLG Patient Problem: Cognitive Changes Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 03/30/2023
ABBOTT DIABETES CARE LTD FREESTYLE LIBRE 3 03/29/2023
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 03/24/2023
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 03/21/2023
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 02/28/2023
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 02/22/2023
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 02/08/2023
ABBOTT DIABETES CARE INC LIBRE 2 SENSOR FREESTYLE 09/27/2022
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2 07/29/2022
BIGFOOT BIOMEDICAL, INC. BIGFOOT UNITY DIABETES MANAGEMENT SYSTEM 07/15/2022
-
-