MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY

MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY is an FDA 510(k)-cleared medical device (K072061) manufactured by Viasys Healthcare GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 21, 2008. Regulation: 8.