Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
153 records meeting your search criteria returned- Product Code: NIK Patient Problem: Swelling Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ASSURA MP ICD 03/07/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ASSURA (DDQP+) 03/06/2017
ST. JUDE MEDICAL, INC. QUARTET 02/16/2017
MEDTRONIC PUERTO RICO OPERATIONS CO. AMPLIA MRI QUAD CRT-D 02/09/2017
GUIDANT CRM CLONMEL IRELAND INOGEN 01/20/2017
GUIDANT CRM CLONMEL IRELAND DYNAGEN 01/11/2017
ST. JUDE MEDICAL, INC. UNIFY ASSURA CRT-D RF HV 01/09/2017
BIOTRONIK SE & CO. KG LUMAX 540 HF-T 12/29/2016
BIOTRONIK SE & CO. KG ITREVIA 7 HF-T QP DF4 IS4 12/29/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. VIVA S 12/09/2016
-
-