CO BREATH ANALYSIS MODULE & MONOXOL II

CO BREATH ANALYSIS MODULE & MONOXOL II is an FDA 510(k)-cleared medical device (K952694) manufactured by Bacharach, 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 January 28, 1996. Regulation: 8.