HITEMP. TM 2 LOOPTIP CAUTERY

HITEMP. TM 2 LOOPTIP CAUTERY is an FDA 510(k)-cleared medical device (K802942) manufactured by Medical Products Development, Inc.. 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 February 3, 1981. Regulation: 8.