• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
114 records meeting your search criteria returned- Product Code: FMG Report Date From: 1/1/2017 Report Date To: 12/31/2017

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITHS MEDICAL ASD, INC. MEDEX¿ LARGE BORE - HI-FLO¿ STOPCOCK 06/28/2017
BAXTER HEALTHCARE - CARTAGO CLEARLINK CONTINU-FLO STOPCOCK AND I.V. 06/21/2017
BAXTER HEALTHCARE - CARTAGO CLEARLINK CONTINU-FLO STOPCOCK AND I.V. 06/21/2017
BAXTER HEALTHCARE - CARTAGO CLEARLINK CONTINU-FLO STOPCOCK AND I.V. 06/21/2017
SMITHS MEDICAL ASD, INC. MEDEX¿ LARGE BORE - HI-FLO¿ STOPCOCK 06/19/2017
SMITHS MEDICAL ASD, INC. MEDEX 05/26/2017
SMITHS MEDICAL ASD, INC. MEDEX¿ SMALL BORE STOPCOCKS 05/22/2017
BAXTER HEALTHCARE - DOMINICAN REPUBLIC STOPCOCK 05/12/2017
BAXTER HEALTHCARE - DOMINICAN REPUBLIC STOPCOCK 05/12/2017
BAXTER HEALTHCARE - DOMINICAN REPUBLIC STOPCOCK 05/11/2017
-
-