MASTERLAB PFT AND MASTERLAB BODY BOX

MASTERLAB PFT AND MASTERLAB BODY BOX is an FDA 510(k)-cleared medical device (K893420) manufactured by Quinton, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 1989. Regulation: 8.