Medical Device Manufacturer · IE , Galway

Arravasc Limited - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

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.

Arravasc Limited is one of 45 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Arravasc Limited

2 devices

1-2 of 2