• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
 
86 records meeting your search criteria returned- Product Code: QKO Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECKMAN COULTER ACCESS SARS-COV-2 IGG II 08/03/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG (1ST IS) 08/02/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG (1ST IS) 07/30/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG II 07/22/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG II 07/21/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG II 07/19/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG II 07/19/2021
BECKMAN COULTER ACCESS SARS-COV-2 IGG II 07/19/2021
DIASORIN S.P.A. LIAISON SARS-COV-2 S1/S2 IGM 06/13/2021
DIASORIN S.P.A. LIAISON SARS-COV-2 S1/S2 IGM 06/13/2021
-
-