NEONATAL CANNULA CAP

NEONATAL CANNULA CAP is an FDA 510(k)-cleared medical device (K864883) manufactured by Behan & Taylor Ent.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 1987. Regulation: 8.