BONART ART-E1 ELECTROSURGERY UNIT

BONART ART-E1 ELECTROSURGERY UNIT is an FDA 510(k)-cleared medical device (K020080) manufactured by Diagnostic Data, 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 February 18, 2002. Regulation: 8.