TWO-WAY ANESTHESIA FILTER

TWO-WAY ANESTHESIA FILTER is an FDA 510(k)-cleared medical device (K790896) manufactured by Pharmaseal Div., Baxter Healthcare Corp.. 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 4, 1979. Regulation: 8.