LATERAL SPINE DETERMAINATIONS DPX/DPX-L/DPX-ALPHA

LATERAL SPINE DETERMAINATIONS DPX/DPX-L/DPX-ALPHA is an FDA 510(k)-cleared medical device (K905291) 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 August 8, 1991. Regulation: 8.