INTERTECH UNIVERSAL HYDROPHOBIC FILTER

INTERTECH UNIVERSAL HYDROPHOBIC FILTER is an FDA 510(k)-cleared medical device (K890346) manufactured by Intertech/Ohio. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 1989. Regulation: 8.