PERCUSSIONAIRE RESPIRATORS (MULTIPLE)

PERCUSSIONAIRE RESPIRATORS (MULTIPLE) is an FDA 510(k)-cleared medical device (K884832) manufactured by Percussionaire Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 1989. Regulation: 8.