SECURCUT ASPIRATION BIOPSY NEEDLE

SECURCUT ASPIRATION BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K013071) manufactured by H.S. Hospital Services S.P.A.. 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 December 11, 2001. Regulation: 8.