PHOENIX EPIDURAL & SPINAL NEEDLES

PHOENIX EPIDURAL & SPINAL NEEDLES is an FDA 510(k)-cleared medical device (K990519) manufactured by Myco Medical Supplies, 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 June 1, 2000. Regulation: 8.