CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS

CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS is an FDA 510(k)-cleared medical device (K931670) manufactured by Carapace, 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 24, 1994. Regulation: 8.