LAP-WAVE 3000 (P07)

LAP-WAVE 3000 (P07) is an FDA 510(k)-cleared medical device (K990732) manufactured by W.O.M. World of Medicine GmbH. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 1999. Regulation: 8.