MICROSURGE VERESS NEEDLE

MICROSURGE VERESS NEEDLE is an FDA 510(k)-cleared medical device (K954520) manufactured by Microsurge, 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 October 15, 1995. Regulation: 8.