Incoba Ltd D/B/A Dynaris - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Incoba Ltd D/B/A Dynaris has 1 FDA 510(k) cleared medical devices. Based in Chesterfield, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Incoba Ltd D/B/A Dynaris Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Incoba Ltd D/B/A Dynaris
1 devices