PRESSURE LIMITING ELBOW WITH MANOMETER PORT

PRESSURE LIMITING ELBOW WITH MANOMETER PORT is an FDA 510(k)-cleared medical device (K911298) manufactured by Intertech Resources, 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 June 24, 1991. Regulation: 8.