DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET

DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET is an FDA 510(k)-cleared medical device (K132202) manufactured by Enthermics Medical Systems, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 5, 2013. Regulation: 8.