MANAN MENGHINI NEEDLE

MANAN MENGHINI NEEDLE is an FDA 510(k)-cleared medical device (K851836) manufactured by Manan Manufacturing Co., Inc.. 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 June 20, 1985. Regulation: 8.