Medical Device Manufacturer · IE , Galway

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

7 submissions · 7 cleared · Since 2008

Total

Cleared

Denied

Brivant, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Galway, IE.

Historical record: 7 cleared submissions from 2008 to 2012. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Brivant, Ltd. Filter by specialty or product code using the sidebar.

Brivant, Ltd. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.

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

7 devices

1-7 of 7