• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
104 records meeting your search criteria returned- Product Code: NIK Patient Problem: Staphylococcus Aureus Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GUIDANT CRM CLONMEL IRELAND INOGEN 04/26/2016
CPI - DEL CARIBE EASYTRAK 2 04/25/2016
CPI - DEL CARIBE EASYTRAK 2 04/25/2016
CPI - DEL CARIBE EASYTRAK 2 01/19/2016
CPI - DEL CARIBE EASYTRAK 2 01/19/2016
CPI - DEL CARIBE EASYTRAK 2 01/18/2016
GUIDANT CRM CLONMEL IRELAND DYNAGEN 01/15/2016
BIOTRONIK SE & CO. KG LUMAX 540 HF-T 11/24/2015
GUIDANT CRM CLONMEL IRELAND INOGEN 10/25/2015
CPI - DEL CARIBE EASYTRAK 2 10/25/2015
-
-