KERR HERCULITE DENTAL COMPOSITE RESTORATIVE MATERI

KERR HERCULITE DENTAL COMPOSITE RESTORATIVE MATERI is an FDA 510(k)-cleared medical device (K844662) manufactured by Kerr Corporation (Danbury). 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 24, 1985. Regulation: 8.