THERAPAX DXT 300 MODEL HF-300

THERAPAX DXT 300 MODEL HF-300 is an FDA 510(k)-cleared medical device (K973315) manufactured by Pantak, 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 December 1, 1997. Regulation: 8.