PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MIN

PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MIN is an FDA 510(k)-cleared medical device (K900315) 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 October 25, 1990. Regulation: 8.