• 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 
 3 
 > 
 
28 records meeting your search criteria returned- Product Code: JTO Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMERIEUX, SA API® RAPID ID 32 STREP 12/21/2017
BIOMERIEUX, SA API® RAPID ID 32 STREP 12/21/2017
BIOMERIEUX, INC VITEK® 2 NH TEST KIT 05/01/2017
BIOMERIEUX, INC VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TE 04/05/2017
BIOMERIEUX, INC VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TE 03/03/2017
BIOMERIEUX, INC VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TE 03/01/2017
BIOMERIEUX, INC VITEK® 2 GRAM-NEGATIVE IDENTIFICATION TE 02/28/2017
BIOMERIEUX, INC VITEK® 2 GN TEST KIT 01/06/2017
BIOMERIEUX, INC VITEK® 2 GN TEST KIT 12/29/2016
BIOMERIEUX INC. VITEK® 2 GN ID TEST KIT 12/22/2016
-
-