Medical Device Manufacturer · US , Danvers , MA

Neurologica Corporation, A Subsidiary OF - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Neurologica Corporation, A Subsidiary OF has 1 FDA 510(k) cleared medical devices. Based in Danvers, US.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Neurologica Corporation, A Subsidiary OF

1 devices

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