TUOHY EPIDURAL NEEDLES

TUOHY EPIDURAL NEEDLES is an FDA 510(k)-cleared medical device (K961152) manufactured by Hakko Shoji Co., Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 1997. Regulation: 8.