NOVOSTE PULSE PLUS BLOOD CONTAINMENT DEVICE

NOVOSTE PULSE PLUS BLOOD CONTAINMENT DEVICE is an FDA 510(k)-cleared medical device (K942977) manufactured by Novoste 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 December 27, 1995. Regulation: 8.