MONOJECT SOFT TISSUE BIOPSY NEEDLE

MONOJECT SOFT TISSUE BIOPSY NEEDLE is an FDA 510(k)-cleared medical device (K834249) manufactured by Sherwood Medical Co.. 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 11, 1984. Regulation: 8.