CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL)

CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL) is an FDA 510(k)-cleared medical device (K973919) manufactured by Medental Intl.. 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 15, 1997. Regulation: 8.