D'AMICO\PEYMAN FLUTED ENDOPROBE

D'AMICO\PEYMAN FLUTED ENDOPROBE is an FDA 510(k)-cleared medical device (K933211) manufactured by Iriderm Div.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 18, 1994. Regulation: 8.