Neuravi, Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neuravi, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Galway, IE.
Last cleared in 2021. Active since 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuravi, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Neuravi, Ltd.
4 devices
Cleared
Oct 13, 2021
EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device
Neurology
30d
Cleared
Jul 30, 2021
EMBOTRAP III Revascularization Device
Neurology
88d
Cleared
Jul 14, 2020
EMBOTRAP III Revascularization Device
Neurology
253d
Cleared
May 09, 2018
EmboTrap ll Revascularization Device
Neurology
184d