G-MM, MODEL 10038

G-MM, MODEL 10038 is an FDA 510(k)-cleared medical device (K021894) manufactured by Vitrolife Sweden AB. 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 September 5, 2002. Regulation: 8.