HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX

HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX is an FDA 510(k)-cleared medical device (K893133) manufactured by Mennen Medical, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 13, 1989. Regulation: 8.