POLYESTER CARDIOTOMY RESERVOIR, FILTERED & UNFILTE

POLYESTER CARDIOTOMY RESERVOIR, FILTERED & UNFILTE is an FDA 510(k)-cleared medical device (K844803) manufactured by Electromedics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 28, 1985. Regulation: 8.