SARNS 8000 MODULAR PERFUSION SYSTEM

SARNS 8000 MODULAR PERFUSION SYSTEM is an FDA 510(k)-cleared medical device (K915183) manufactured by 3M Health Care, Sarns. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 7, 1992. Regulation: 8.