RESPIRONICS' DIGITAL MANOMETER

RESPIRONICS' DIGITAL MANOMETER is an FDA 510(k)-cleared medical device (K904935) manufactured by Respironics, 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 April 2, 1991. Regulation: 8.