DEKA Infusion System, DEKA Administration Set

DEKA Infusion System, DEKA Administration Set is an FDA 510(k)-cleared medical device (K232316) manufactured by Deka Research and Development. 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 February 29, 2024. Regulation: 8.