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
 

 
 < 
 1 
 2 
 3 
 4 
 > 
 
33 records meeting your search criteria returned- Product Code: MHX Product Problem: Use of Incorrect Control/Treatment Settings Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SPACELABS HEALTHCARE INC. SPACELABS ULTRAVIEW SL2600 COMPACT MONIT 01/31/2018
SPACELABS HEALTHCARE INC. SPACELABS ULTRAVIEW SL2400 COMPACT MONIT 01/31/2018
NIHON KOHDEN CORPORATION CNS-6201A 01/23/2018
NIHON KOHDEN CORPORATION CNS-6201A 11/30/2017
NIHON KOHDEN CORPORATION CNS-9700A 11/30/2017
SPACELABS HEALTHCARE INC. SPACELABS ULTRAVIEW PATIENT MONITOR 06/14/2017
PHILIPS MEDICAL SYSTEMS M3150 UPGRADE REL N.0 01/04/2017
NKUS LAB RNS-9703-019 03/15/2016
MORTARA INSTRUMENT, INC SURVEYOR CENTRAL 02/25/2016
MORTARA INSTRUMENT, INC SURVEYOR CENTRAL 02/25/2016
-
-