THORAX FD AND MULTIX FD

THORAX FD AND MULTIX FD is an FDA 510(k)-cleared medical device (K983732) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 20, 1999. Regulation: 8.