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 
 13 
 14 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MINDRAY DS USA, INC. MINDRAY 17M PATIENT MONITOR AND MINDRAY 02/22/2022
MINDRAY DS USA, INC. MINDRAY 17M PATIENT MONITOR AND MINDRAY 02/22/2022
NIHON KOHDEN CORPORATION CNS-6801A 02/22/2022
NIHON KOHDEN CORPORATION CNS-6801A 02/18/2022
NIHON KOHDEN CORPORATION CNS-6201A 02/04/2022
NIHON KOHDEN CORPORATION CNS-9700A 01/20/2022
NIHON KOHDEN CORPORATION CNS-6801A 12/29/2021
NIHON KOHDEN CORPORATION CNS-6801A 12/29/2021
SPACELABS HEALTHCARE INC. SPACELABS XHIBIT CENTRAL STATION 12/10/2021
PHILIPS NORTH AMERICA LLC. PHILIPS CARDIAC MONITOR 12/06/2021
-
-