Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0)

Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) is an FDA 510(k)-cleared medical device (K232923) manufactured by Varian Medical Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 2024. Regulation: 8.