G-MOPS, MODEL 10030

G-MOPS, MODEL 10030 is an FDA 510(k)-cleared medical device (K021893) 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.