DISCOID/CLEOID DOUBLE END AMALGAM CARVER

DISCOID/CLEOID DOUBLE END AMALGAM CARVER is an FDA 510(k)-cleared medical device (K901177) manufactured by American Medical Ceramics, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 15, 1990. Regulation: 8.