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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
163 records meeting your search criteria returned- Product Code: FMG Report Date From: 1/1/2018 Report Date To: 12/31/2018

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITHS MEDICAL ASD, INC. MEDEX 08/02/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA¿ 3-WAY STOPCOCKS 08/01/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA¿ PLUS 3-WAY STOPCOCK 08/01/2018
ICU MEDICAL, INC. ICU MEDICAL 07/30/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA¿ STOPCOCKS CONNECTA PLUS 07/27/2018
BAXTER HEALTHCARE - MALTA STOPCOCK 07/24/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA¿ STOPCOCK 07/20/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA ¿ EXTENSION TUBE 07/17/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA¿ STOPCOCKS CONNECTA PLUS 07/12/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD CONNECTA¿ STOPCOCK 07/12/2018
-
-