Neurescue Aps - FDA 510(k) Cleared Devices

Neurescue Aps has 1 FDA 510(k) cleared medical devices. Based in Copenhagen, DK.

Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.

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

510(k) submissions have been managed by CardioMed Device Consultants, LLC as regulatory consultant.