RESOUND ENDOSCOPIC ULTRASOUND ASPIRATION NEEDLE

RESOUND ENDOSCOPIC ULTRASOUND ASPIRATION NEEDLE is an FDA 510(k)-cleared medical device (K100712) manufactured by Boston Scientific 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 March 29, 2010. Regulation: 8.