VENTILARM II PORTABLE AIRWAY PRESSURE MONITOR

VENTILARM II PORTABLE AIRWAY PRESSURE MONITOR is an FDA 510(k)-cleared medical device (K895747) manufactured by Hudson Oxygen Therapy Sales Co.. 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 26, 1989. Regulation: 8.