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 
 > 
 
18 records meeting your search criteria returned- Product Code: LOK Report Date From: 1/1/2019 Report Date To: 12/31/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT IRELAND DIAGNOSTICS DIVISION ARCHITECT AFP 12/26/2019
ABBOTT IRELAND ARCHITECT AFP 12/19/2019
ABBOTT IRELAND ARCHITECT AFP 11/22/2019
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE 2000 XPI - AFP 11/15/2019
ABBOTT IRELAND ARCHITECT AFP 09/03/2019
ABBOTT IRELAND ARCHITECT AFP 08/21/2019
ABBOTT IRELAND ARCHITECT AFP 08/12/2019
ABBOTT IRELAND ARCHITECT AFP 06/09/2019
ABBOTT IRELAND ARCHITECT AFP 06/07/2019
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ATELLICA IM 1300 ALPHA FETOPROTEIN (AFP) 05/29/2019
-
-