COMPANION 2800A PORTABLE VENTILATOR - MODIFICATION

COMPANION 2800A PORTABLE VENTILATOR - MODIFICATION is an FDA 510(k)-cleared medical device (K873215) manufactured by Puritan Bennett 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 January 21, 1988. Regulation: 8.