ELECATH PULSATILE PERFUSION PUMP

ELECATH PULSATILE PERFUSION PUMP is an FDA 510(k)-cleared medical device (K854975) manufactured by Electro-Catheter Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 14, 1986. Regulation: 8.