HORIZONS CYTOLOGY BRUSH

HORIZONS CYTOLOGY BRUSH is an FDA 510(k)-cleared medical device (K021998) manufactured by Horizons Intl. Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 11, 2002. Regulation: 8.