JOSTRA HL-20 INTEGRATED PERFUSION SYSTEM

JOSTRA HL-20 INTEGRATED PERFUSION SYSTEM is an FDA 510(k)-cleared medical device (K943803) manufactured by Janus Biomedical, 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 29, 1996. Regulation: 8.