Artis zee/zeego & Artis Q/Q.zen

Artis zee/zeego & Artis Q/Q.zen is an FDA 510(k)-cleared medical device (K181407) manufactured by Siemens Medical Solution USA, 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 August 14, 2018. Regulation: 8.