Medical Device Manufacturer · IE , Galway

Arravasc, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016

Total

Cleared

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.

Arravasc, Ltd. is one of 89 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Arravasc, Ltd.

2 devices

1-2 of 2