MARLOW VERRES NEEDLES

MARLOW VERRES NEEDLES is an FDA 510(k)-cleared medical device (K913586) manufactured by Marlo Surgical Technology. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 7, 1991. Regulation: 8.