ATRIUM 2052 CHEST DRAIN, DUAL COLLECTION BLOOD

ATRIUM 2052 CHEST DRAIN, DUAL COLLECTION BLOOD is an FDA 510(k)-cleared medical device (K897127) manufactured by Atrium Medical Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 1990. Regulation: 8.