• 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 
 10 
 > 
 
108 records meeting your search criteria returned- Product Code: LQL Product Problem: Incorrect, Inadequate or Imprecise Result or Readings Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMERIEUX, INC. VITEK® 2 GP ID TEST KIT 10/29/2018
BIOMERIEUX INC. VITEK® 2 GRAM-POSITIVE (GP) IDENTIFICATI 10/15/2018
BIOMERIEUX, INC. VITEK® 2 GRAM POSITIVE ID TEST KIT 10/11/2018
BIOMERIEUX, INC. VITEK® 2 GP (GRAM-POSITIVE) ID TEST KIT 10/09/2018
BIOMERIEUX, INC. VITEK® 2 GP ID CARD 10/03/2018
BIOMERIEUX, INC. VITEK® 2 GRAM POSITIVE ID TEST KIT 09/24/2018
BIOMERIEUX, INC. VITEK® 2 GRAM POSITIVE ID TEST KIT 09/24/2018
BIOMERIEUX, INC. VITEK® 2 GP ID TEST KIT 09/18/2018
BIOMERIEUX, INC. VITEK® 2 GP TEST KIT 09/06/2018
BIOMERIEUX, INC. VITEK® 2 GP TEST KIT 08/31/2018
-
-