HOLLOW FIBER MEMBRANE OYGENATOR QUADROX HMO 1010

HOLLOW FIBER MEMBRANE OYGENATOR QUADROX HMO 1010 is an FDA 510(k)-cleared medical device (K992559) manufactured by Jostra Bentley. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 1999. Regulation: 8.