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 
 12 
 > 
 
118 records meeting your search criteria returned- Product Code: LGD Report Date From: 1/1/2023 Report Date To: 12/31/2023

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS ELECSYS TOXO IGM 03/28/2023
ROCHE DIAGNOSTICS ELECSYS TOXO IGM 03/23/2023
ROCHE DIAGNOSTICS ELECSYS TOXO IGM 03/23/2023
ABBOTT GMBH ALINITY I TOXO IGG REAGENT KIT 03/23/2023
BIOMÉRIEUX SA VIDAS® TOXO IGM 03/21/2023
ROCHE DIAGNOSTICS ELECSYS TOXO IGM 03/17/2023
ABBOTT GMBH ALINITY I TOXO IGG REAGENT KIT 03/16/2023
ABBOTT GMBH ALINITY I TOXO IGG REAGENT KIT 03/13/2023
ROCHE DIAGNOSTICS ELECSYS TOXO IGM 03/13/2023
ROCHE DIAGNOSTICS ELECSYS TOXO IGM 03/06/2023
-
-