SHILEY FENESTRATED REUSABLE INNER CANNULA, MODIF

SHILEY FENESTRATED REUSABLE INNER CANNULA, MODIF is an FDA 510(k)-cleared medical device (K930895) manufactured by Mallinckrodt Medical Tpi, 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 1, 1993. Regulation: 8.