DATASCOPE PERCOR=DL DUAL-LUMEN INTRA

DATASCOPE PERCOR=DL DUAL-LUMEN INTRA is an FDA 510(k)-cleared medical device (K810297) manufactured by Datascope 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 May 5, 1981. Regulation: 8.