RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.)

RESPIRONICS BIPAP PRESSURE ALARM (BIPAP P.A.) is an FDA 510(k)-cleared medical device (K902276) 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 August 16, 1990. Regulation: 8.