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
 

 
 
 1 
 2 
 > 
 
12 records meeting your search criteria returned- Product Code: JAA Product Problem: Device Alarm System Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS MEDICAL SOLUTIONS USA, INC. ARTIS VD 11C 02/06/2020
GE (OEM) HEALTHCARE SURGERY SURGICAL C-ARM 03/15/2019
PHILIPS MEDICAL SYSTEMS PHILLIPS IGT ALLURA FD ESSENTIALS 28 07/05/2018
GE OEC MEDICAL SYSTEMS (SLC) 9900 03/26/2015
GE OEC MEDICAL SYSTEMS (SLC) 9900 02/16/2015
GE OEC MEDICAL SYSTEMS (SLC) 9800 09/04/2014
GE OEC MEDICAL SYSTEMS (SLC) 9800 07/23/2014
GE OEC MEDICAL SYSTEMS (SLC) 9900 06/27/2014
GE OEC MEDICAL SYSTEMS (SLC) 9800 05/02/2014
GE OEC MEDICAL SYSTEMS (SLC) 9900 04/15/2014
-
-