Neurologica Corporation - FDA 510(k) Cleared Devices

Neurologica Corporation has 8 FDA 510(k) cleared medical devices. Based in Danvers, US.

Latest FDA clearance: Sep 2025. Active since 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Neurologica Corporation Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.