Systemsone is one of 24542 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Systemsone - FDA 510(k) Cleared Devices
Recent clearances: ELECTROPHYSIOLOGY SYSTEMS INTEGRATOR (EPSI)
1
Total
1
Cleared
0
Denied
Systemsone has 1 FDA 510(k) cleared medical devices. Based in Anchorage, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Systemsone Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Systemsone
1 devices