ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER

ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER is an FDA 510(k)-cleared medical device (K972595) manufactured by Avid N.I.T., 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 May 19, 1998. Regulation: 8.