• 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
 

 
 
8 records meeting your search criteria returned- Product Code: LLZ Product Problem: Device Inoperable Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS PHILIPS MEDICAL SYSTEM 07/31/2019
GE OEC MEDICAL SYSTEMS (SLC) IT3500 02/10/2017
GE OEC MEDICAL SYSTEMS (SLC) ENTRAK 11/04/2016
GE OEC MEDICAL SYSTEMS (SLC) ITRAK 3000 07/19/2016
GE OEC MEDICAL SYSTEMS (SLC) ITRAK 3500 05/19/2016
GE OEC MEDICAL SYSTEMS (SLC) ENTRAK 2500 11/05/2015
GE OEC MEDICAL SYSTEMS (SLC) ENTRAK 2500 08/24/2015
Unknown Manufacturer ENTRAK 2500 07/01/2015
-
-