MONA LISA ASPIRATION NEEDLE

MONA LISA ASPIRATION NEEDLE is an FDA 510(k)-cleared medical device (K032208) manufactured by Fertility Technology Resources, Inc.. 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 December 8, 2003. Regulation: 8.