• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
132 records meeting your search criteria returned- Product Code: NIK Patient Problem: Purulent Discharge Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION EASYTRAK 2 11/19/2018
BOSTON SCIENTIFIC CORPORATION DYNAGEN CRT-D 11/05/2018
BOSTON SCIENTIFIC CORPORATION INOGEN X4 CRT-D 10/24/2018
GUIDANT CRM CLONMEL IRELAND DYNAGEN 10/22/2018
GUIDANT CRM CLONMEL IRELAND VIGILANT 10/18/2018
MEDTRONIC MED REL MEDTRONIC PUERTO RICO CONSULTA CRT-D 08/07/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. AMPLIA MRI QUAD CRT-D 07/16/2018
GUIDANT CRM CLONMEL IRELAND DYNAGEN 04/10/2018
CPI - DEL CARIBE EASYTRAK 2 01/17/2018
GUIDANT CRM CLONMEL IRELAND DYNAGEN 01/17/2018
-
-