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
 

 
 
6 records meeting your search criteria returned- Product Code: JAK Product Problem: Inadequate or Insufficient Training Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NEUROLOGICA CORPORATION NL5000 10/30/2023
NEUROLOGICA CORPORATION OMNITOM 11/19/2021
NEUROLOGICA CORPORATION OMNITOM 07/31/2021
SIEMENS HEALTHCARE GMBH SOMATOM GO.ALL 05/25/2021
SIEMENS HEALTHCARE GMBH SOMATOM GO.UP 05/21/2021
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC. BRILLANCE 16 AIR 11/25/2014
-
-