Medical Device Manufacturer · US , Danvers , MA

Neurologica Corporation - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2005

Total

Cleared

Denied

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.

FDA 510(k) Regulatory Record - Neurologica Corporation

8 devices

1-8 of 8