Archeon - FDA 510(k) Cleared Devices

Archeon has 1 FDA 510(k) cleared medical devices. Based in Besan?on, FR.

Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.

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

510(k) submissions have been managed by Gloster Biomedical International, LLC as regulatory consultant.