PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST

PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST is an FDA 510(k)-cleared medical device (K875313) manufactured by Bisco, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 9, 1988. Regulation: 8.