SINGLE USE ASPIRATION NEEDLE NA-201SX-4022

SINGLE USE ASPIRATION NEEDLE NA-201SX-4022 is an FDA 510(k)-cleared medical device (K050503) manufactured by Olympus Medical Systems Corporation. 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 May 11, 2005. Regulation: 8.