MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE

MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE is an FDA 510(k)-cleared medical device (K011283) manufactured by The Kendall Company. 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 October 14, 2001. Regulation: 8.