Arravasc Limited is one of 89 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Arravasc Limited - FDA 510(k) Cleared Devices
Recent clearances: Pirouette 035, Pirouette 018
2
Total
2
Cleared
0
Denied
Arravasc Limited has 2 FDA 510(k) cleared medical devices. Based in Galway, IE.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arravasc Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Arravasc Limited
2 devices