KLS MARTIN ELECTROSURGICAL INSTRUMENTS

KLS MARTIN ELECTROSURGICAL INSTRUMENTS is an FDA 510(k)-cleared medical device (K082505) manufactured by Kl Martin L.P.. 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 June 11, 2009. Regulation: 8.