• 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 
 3 
 4 
 > 
 
37 records meeting your search criteria returned- Product Code: JAA Report Date From: 1/1/2018 Report Date To: 12/31/2018

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
Unknown Manufacturer FLUOROSCOPY EXAM 12/26/2018
SIEMENS HEALTHCARE GMBH BIPLANE INTERVASCULAR IMAGING DEVICE 12/19/2018
GE MEDICAL SYSTEMS LLC INNOVA 12/19/2018
TOSHIBA-CANON MEDICAL SYSTEMS USA, INC. TOSHIBA-CANON INFINIX- 1 12/06/2018
GE MEDICAL SYSTEMS, LLC PRESTIGE SI 11/29/2018
Unknown Manufacturer unknown brand name 11/15/2018
Unknown Manufacturer unknown brand name 11/15/2018
Unknown Manufacturer unknown brand name 11/15/2018
Unknown Manufacturer unknown brand name 11/15/2018
PHILIPS MEDICAL SYSTEMS SYSTEM, X-RAY, FLUOROSCOPIC 10/31/2018
-
-