NEOMED ORAL/ENTERAL SYRINGE

NEOMED ORAL/ENTERAL SYRINGE is an FDA 510(k)-cleared medical device (K122373) manufactured by Neomed, 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 September 19, 2012. Regulation: 8.