• 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 
 3 
 > 
 
25 records meeting your search criteria returned- Product Code: KST Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION BLOOD COLLECTION DEVICE W/MALE LUER 02/12/2016
CAREFUSION BLOOD COLLECTION DEVICE W/MALE LUER 02/12/2016
CAREFUSION BLOOD COLLECTION DEVICE W/MALE LUER 01/25/2016
CAREFUSION BLOOD COLLECTION DEVICE 10/30/2015
HUMMINGBIRD MEDICAL DEVICES, INC HUMMI 10/27/2015
CAREFUSION BLOOD COLLECTION DEVICE 10/10/2015
CAREFUSION BLOOD COLLECTION DEVICE 10/02/2015
Unknown Manufacturer HUMMI 08/13/2015
CAREFUSION BLOOD COLLECTION DEVICE 08/13/2015
CAREFUSION BLOOD COLLECTION DEVICE 08/13/2015
-
-