• 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 
 
 
21 records meeting your search criteria returned- Product Code: LON Product Problem: False Negative Result Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMERIEUX, INC. VITEK 2 AST-GP78 TEST KIT 03/18/2020
BIOMERIEUX, INC. VITEK® 2 AST-GP75 TEST KIT 09/16/2019
BIOMERIEUX, INC. VITEK® 2 AST-P657 TEST KIT 08/02/2019
BIOMERIEUX, INC. VITEK® 2 AST-P644 TEST KIT 07/18/2019
BIOMERIEUX INC. VITEK®2 AST-GN67 TEST KIT 04/19/2018
BIOMERIEUX INC. VITEK® 2 AST-XN05 12/22/2017
BIOMERIEUX INC. VITEK®2 AST-N303 TEST KIT 11/16/2017
BIOMERIEUX, INC VITEK® 2 AST-P631 TEST KIT 06/09/2017
BIOMERIEUX, INC VITEK® 2 ANTIMICROBIAL SUSCEPTIBILITY TE 09/14/2015
BIOMERIEUX, INC VITEK 2 AST-N284 TEST KIT 07/13/2015
-
-