Kontron Medical Systems Sas is one of 22808 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kontron Medical Systems Sas - FDA 510(k) Cleared Devices
Recent clearances: SIGMA 5000 SERIES, IMAGIC, SIGMA 5000 SERIES IMAGIC ULTRASOUND SYSTEM, SIGMA 5000 SERIES IMAGIC ULTRASOUND SYSTEM
4
Total
4
Cleared
0
Denied
Kontron Medical Systems Sas has 4 FDA 510(k) cleared medical devices. Based in Hasbrouck Heights, US.
Historical record: 4 cleared submissions from 2000 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Kontron Medical Systems Sas Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Kontron Medical Systems Sas
4 devices