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 
 > 
 
18 records meeting your search criteria returned- Product Code: OXO Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM IMAGING SYSTEM 02/05/2024
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM IMAGING SYSTEM 01/08/2024
HOLOGIC, INC. FLOUROCSAN INSIGHT 09/01/2023
SIEMENS MEDICAL SOLUTIONS USA, INC. 51 V SIEMENS ORBIC C-ARM IMAGING SYSTEM 08/12/2023
SIEMENS AG/SIEMENS HEALTHCARE GMBH ARCADIS ORBIC 08/12/2023
SIEMENS MEDICAL SOLUTIONS USA, INC. 51 V SIEMENS ORBIC C-ARM IMAGING SYSTEM 08/12/2023
SIEMENS MEDICAL SOLUTIONS USA, INC. 51 V SIEMENS ORBIC C-ARM IMAGING SYSTEM 08/12/2023
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM IMAGING SYSTEM 08/07/2023
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM IMAGING SYSTEM 04/26/2023
MEDTRONIC NAVIGATION, INC (LITTLETON) O-ARM IMAGING SYSTEM 03/22/2023
-
-