ELECATH INFANT ARTERIAL & VENOUS CANNU

ELECATH INFANT ARTERIAL & VENOUS CANNU is an FDA 510(k)-cleared medical device (K842369) manufactured by Electro-Catheter Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 26, 1984. Regulation: 8.