SPINAL EPIDURAL NEEDLES

SPINAL EPIDURAL NEEDLES is an FDA 510(k)-cleared medical device (K002405) 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 May 31, 2001. Regulation: 8.