Q220F CARDITOMY RESERVOIR/MODIFIED

Q220F CARDITOMY RESERVOIR/MODIFIED is an FDA 510(k)-cleared medical device (K790635) manufactured by Bentley Laboratories, 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 17, 1979. Regulation: 8.