Schiller AG - FDA 510(k) Cleared Devices

Schiller AG has 16 FDA 510(k) cleared cardiovascular devices. Based in Baar, CH.

Last cleared in 2023. Active since 1985.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Arazy Group Consultants, Inc. as regulatory consultant.