THE TULIP MONO-POLAR CAUTERY SPATULA

THE TULIP MONO-POLAR CAUTERY SPATULA is an FDA 510(k)-cleared medical device (K952973) manufactured by The Tulip Mfg. Co.. 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 September 10, 1995. Regulation: 8.