VERSA-KATH EPIDURAL CATHETER, MODEL 156-2124

VERSA-KATH EPIDURAL CATHETER, MODEL 156-2124 is an FDA 510(k)-cleared medical device (K023140) manufactured by Epimed International, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 14, 2003. Regulation: 8.