ACTA-SCANNER R 0200FS

ACTA-SCANNER R 0200FS is an FDA 510(k)-cleared medical device (K770573) manufactured by Pfizer Medical Systems, 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 March 29, 1977. Regulation: 8.