Monaghan medical filtered mouthpiece kit

Monaghan medical filtered mouthpiece kit is an FDA 510(k)-cleared medical device (K220145) manufactured by Monaghan Medical Corporation. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 23, 2023. Regulation: 8.