Arravasc, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Arravasc, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Galway, IE.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arravasc, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arravasc, Ltd.
2 devices