MONOJECT TUOHY POINT EPIDURAL NEEDLE (22G X 3 1/2)

MONOJECT TUOHY POINT EPIDURAL NEEDLE (22G X 3 1/2) is an FDA 510(k)-cleared medical device (K951411) manufactured by Sherwood Medical Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 30, 1995. Regulation: 8.