Agfa N.V. - FDA 510(k) Cleared Devices

Agfa N.V. has 6 FDA 510(k) cleared medical devices. Based in Mortsel, BE.

Last cleared in 2021. Active since 2019. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Agfa N.V. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Agfa US Corp. as regulatory consultant.