VITALOGRAPH - BREATHCO MONITOR

VITALOGRAPH - BREATHCO MONITOR is an FDA 510(k)-cleared medical device (K902113) manufactured by Mcneill Intl., 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 October 25, 1990. Regulation: 8.