• 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 
 > 
 
16 records meeting your search criteria returned- Product Code: JAK Product Problem: No Apparent Adverse Event Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NEUROLOGICA CORPORATION NL5000 03/20/2024
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. IQON SPECTRAL CT 11/16/2023
PHILIPS HEALTHCARE (SUZHOU) CO., LTD. INCISIVE CT 10/12/2023
PHILIPS HEALTHCARE (SUZHOU) CO., LTD. INCISIVE CT 10/12/2023
PHILIPS MEDICAL SYSTEMS TECHNOLOGIES LTD BRILLIANCE 09/28/2023
PHILIPS HEALTHCARE (SUZHOU) CO., LTD. INGENUITY CT 08/13/2023
VERAN MEDICAL TECHNOLOGIES, INC SPIN PLANNING SOFTWARE APPLICATION 06/07/2023
VERAN MEDICAL TECHNOLOGIES, INC SPIN DRIVE SOFTWARE APPLICATION 04/14/2023
VERAN MEDICAL TECHNOLOGIES, INC SPIN DRIVE SOFTWARE APPLICATION 03/03/2023
SIEMENS HEALTHCARE GMBH-CT SOMATOM GO.NOW 10/13/2022
-
-