• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: GGN Product Problem: Use of Device Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ACCRIVA DIAGNOSTICS HEPCHECK P214 NORMAL CONTROL 08/10/2016
ACCRIVA DIAGNOSTICS HEMOCHRON JR. DIRECTCHECK, PT ABNORMAL 07/29/2016
ACCRIVA DIAGNOSTICS DIRECTCHECK, PT ABNORMAL 06/20/2016
ACCRIVA DIAGNOSTICS DIRECTCHECK ACT+ ABNORMAL 05/13/2016
ACCRIVA DIAGNOSTICS DIRECTCHECK QUALITY CONTROL 12/22/2015
INTERNATIONAL TECHNIDYNE CORP. DRECTCHECK QUALITY CONTROL, NORMAL ACT+ 09/15/2015
INTERNATIONAL TECHNIDYNE CORP. DIRECTCHECK QUALITY CONTROL 07/15/2015
INTERNATIONAL TECHNIDYNE CORP. DIRECTCHECK QUALITY CONTROL 04/23/2015
INTERNATIONAL TECHNIDYNE CORP. DIRECTCHECK QUALITY CONTROL 04/03/2015
INTERNATIONAL TECHNIDYNE CORP. DIRECTCHECK QUALITY CONTROL 03/18/2015
-
-