MAGTARAK RESPIRATORY MONITOR & FLOW SENS

MAGTARAK RESPIRATORY MONITOR & FLOW SENS is an FDA 510(k)-cleared medical device (K823555) manufactured by Penlon, 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 4, 1983. Regulation: 8.