KHURI REGIONAL TISSUE PH MONITOR

KHURI REGIONAL TISSUE PH MONITOR is an FDA 510(k)-cleared medical device (K862114) manufactured by Vascular Technology Incorporated. 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, 1986. Regulation: 8.