Propeller Sensor for Neohaler

Propeller Sensor for Neohaler is an FDA 510(k)-cleared medical device (K180770) manufactured by Reciprocal Labs Corporation. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 31, 2018. Regulation: 8.