DPX-L AND DPX-ALPHA, MODIFICATION

DPX-L AND DPX-ALPHA, MODIFICATION is an FDA 510(k)-cleared medical device (K904980) manufactured by Lunar. 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 4, 1990. Regulation: 8.