Endoluminal Occlusion System-EOS

Endoluminal Occlusion System-EOS is an FDA 510(k)-cleared medical device (K150402) manufactured by Artventive Medical Group, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 24, 2015. Regulation: 8.