VITALOGRAPH-BREATHCO MONITOR

VITALOGRAPH-BREATHCO MONITOR is an FDA 510(k)-cleared medical device (K892524) manufactured by Vitalograph , Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 4, 1989. Regulation: 8.