BALLPEN SPINAL NEEDLE W/WO INTRODUCER

BALLPEN SPINAL NEEDLE W/WO INTRODUCER is an FDA 510(k)-cleared medical device (K011122) manufactured by Rusch Intl.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 15, 2001. Regulation: 8.