Aeon Astron Europe B.V. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Aeon Astron Europe B.V. has 3 FDA 510(k) cleared medical devices. Based in Leiden, NL.
Historical record: 3 cleared submissions from 2009 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aeon Astron Europe B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aeon Astron Europe B.V.
3 devices