KENDALL BLUNT TUOHY EPIDURAL NEEDLE

KENDALL BLUNT TUOHY EPIDURAL NEEDLE is an FDA 510(k)-cleared medical device (K954706) manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 29, 1996. Regulation: 8.