• 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 
 3 
 4 
 
 
38 records meeting your search criteria returned- Product Code: DRG Patient Problem: No Information Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ORG-9110A 06/07/2017
NIHON KOHDEN CORPORATION ZM-920PA 04/12/2017
NIHON KOHDEN CORPORATION ZM-930PA 04/11/2017
VISICU, INC ECARECOORDINATOR 10/14/2016
NIHON KOHDEN CORPORATION ORG-9110A 10/13/2016
NKUS LAB CENTRAL MONITORING SYSTEM 10/09/2016
IDEAL LIFE IDEAL LIFE BLOOD PRESSURE MONITOR 07/26/2016
PHILIPS MEDICAL SYSTEMS INTELLIVUE 04/06/2016
-
-