PNEUMOTHERML, MODEL: 5800

PNEUMOTHERML, MODEL: 5800 is an FDA 510(k)-cleared medical device (K092685) manufactured by Salter Labs. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 23, 2009. Regulation: 8.