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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
116 records meeting your search criteria returned- Product Code: FJK Report Date From: 1/1/2014 Report Date To: 12/31/2014

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ERIKA DE REYNOSA, S.A. DE C.V. SINGLE NEEDLE BLOOD TUBING SET 03/12/2014
ERIKA DE REYNOSA, S.A. DE C.V. COMBI SET 03/11/2014
GAMBRO RENAL PRODUCTS S.A. DE C.V. CARTRIDGE 03/04/2014
REYNOSA MFG CUSTOM COMBI SET 02/24/2014
REYNOSA MANUFACTURING CUSTOM COMBI SET W/SPLIT SEPTUM 02/18/2014
FRESENIUS MEDICAL CARE NORTH AMERICA FRESENIUS COMBI SET 2008, NO HEPARIN 02/18/2014
FRESENIUS MEDICAL CARE NORTH AMERICA FRESENIUS COMBISET 2008 02/14/2014
GAMBRO RENAL PRODUCTS S.A. DE C.V. CARTRIDGE 02/12/2014
REYNOSA MANUFACTURING CUSTOM COMBI SET BLOODLINE 02/11/2014
REYNOSA PLANT CUSTOM COMBI SET 02/07/2014
-
-