Brivant Limited (Lake Region Medical) is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Brivant Limited (Lake Region Medical) - FDA 510(k) Cleared Devices
Recent clearances: Hi-Torque Vektor, .014, 195cm, Str, Hi-Torque Vektor, .014, 195cm, J, Hi-Torque Vektor, .014, 300cm, Str, Hi-Torque Vektor, .014, 300cm, J
1
Total
1
Cleared
0
Denied
Brivant Limited (Lake Region Medical) has 1 FDA 510(k) cleared medical devices. Based in Galway, IE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Brivant Limited (Lake Region Medical) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Brivant Limited (Lake Region Medical)
1 devices