VITA VMK MASTER

VITA VMK MASTER is an FDA 510(k)-cleared medical device (K093446) manufactured by Vita Zahnfabrik H. Rauter GmbH & Co. Kg.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 2, 2009. Regulation: 8.