• 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 
 5 
 6 
 > 
 
51 records meeting your search criteria returned- Product Code: JAK Patient Problem: Laceration(s) Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GE MEDICAL SYSTEMS, LLC MAXIMA 03/26/2024
SIEMENS HEALTHCARE GMBH SOMATOM GO.UP 08/10/2023
SIEMENS HEALTHCARE GMBH SOMATOM X.CEED 08/10/2023
GE HEALTHCARE JAPAN CORPORATION REVOLUTION CT 05/16/2023
GE HANGWEI MEDICAL SYSTEMS CO., LTD. CT 750HD 03/01/2023
SIEMENS HEALTHCARE GMBH-CT SOMATOM DRIVE 09/23/2022
MOBIUS IMAGING, LLC AIRO CT SCANNER 09/02/2022
SIEMENS HEALTHCARE GMBH-CT SOMATOM SCOPE 08/25/2022
GE MEDICAL SYSTEMS, LLC MAXIMA 06/17/2022
SIEMENS HEALTHCARE GMBH-CT SOMATOM DRIVE 06/02/2022
-
-