LOPER CELIAC PLEXUS BLOCK CATHETER KIT

LOPER CELIAC PLEXUS BLOCK CATHETER KIT is an FDA 510(k)-cleared medical device (K895955) manufactured by Opticon Medical, 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 February 21, 1990. Regulation: 8.