TE ME NA EPIDURAL CATHETER

TE ME NA EPIDURAL CATHETER is an FDA 510(k)-cleared medical device (K991259) manufactured by Te ME NA S.A.R.L.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 20, 2001. Regulation: 8.