HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES

HORIZONS ANSO TRANSBRONCHIAL ASPIRATION NEEDLES is an FDA 510(k)-cleared medical device (K022546) manufactured by Horizons Intl. Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 2002. Regulation: 8.