SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES

SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES is an FDA 510(k)-cleared medical device (K983858) manufactured by Sims Portex, 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 January 28, 1999. Regulation: 8.