MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR

MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR is an FDA 510(k)-cleared medical device (K920166) manufactured by Conmedcorp. 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 November 5, 1992. Regulation: 8.