• 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
 

 
 
4 records meeting your search criteria returned- Product Code: LNH Patient Problem: Misdiagnosis Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HITACHI LTD, HEALTHCARE BUSINESS UNIT AIRIS ELITE MR SYSTEM 08/05/2020
HITACHI LTD, HEALTHCARE BUSINESS UNIT ALTAIRE MR SYSTEM 04/09/2020
HITACHI MEDICAL CORPORATION ELITE 03/12/2019
SIEMENS HEALTHCARE GMBH MAGNETOM SKYRA 11/02/2017
-
-