EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)

EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y) is an FDA 510(k)-cleared medical device (K904685) manufactured by Exel Intl.. 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 November 20, 1990. Regulation: 8.