INTERPULSE MEMBRANE OXYGENATION SYSTEM

INTERPULSE MEMBRANE OXYGENATION SYSTEM is an FDA 510(k)-cleared medical device (K803003) manufactured by Extracorporeal Medical Specialities, 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 January 21, 1981. Regulation: 8.