BEAVERS' DENTAL DIAMOND INSTRUMENTS

BEAVERS' DENTAL DIAMOND INSTRUMENTS is an FDA 510(k)-cleared medical device (K880179) manufactured by Beavers Dental, Div. Sybron Canada, Ltd.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 8, 1988. Regulation: 8.