SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313

SUNLAMP, FLOURESCENT DERMATRON F40-313 AND F20-313 is an FDA 510(k)-cleared medical device (K760519) manufactured by Dermatron Corp.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 1976. Regulation: 8.