• 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: FEG Report Date From: 1/1/2017 Report Date To: 12/31/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (COVINGTON) -1018233 BARD® NASOGASTRIC SUMP TUBE WITH PREVENT 12/04/2017
COVIDIEN KANGAROO 11/30/2017
COVIDIEN LP SALEM SUMP 11/13/2017
C.R. BARD, INC. (COVINGTON) -1018233 BARD® NASOGASTRIC SUMP TUBE WITH PREVENT 08/31/2017
C.R. BARD, INC. (COVINGTON) -1018233 BARD® NASOGASTRIC SUMP TUBE WITH PREVENT 08/31/2017
MITG - KENMEX SALEM SUMP 08/02/2017
COVIDIEN LP SALEM SUMP 06/22/2017
COVIDIEN MEDTRONIC COVIDIEN SALEM SUMP DUAL LUMEN STOMACH T 04/27/2017
COVIDIEN MEDTRONIC COVIDIEN SALEM SUMP DUAL LUMEN STOMACH T 04/27/2017
COVIDIEN SALEM SUMP 04/18/2017
-
-