SORENSON CATALOG #IFL-120S

SORENSON CATALOG #IFL-120S is an FDA 510(k)-cleared medical device (K811228) manufactured by Sorensen Research. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 8, 1981. Regulation: 8.