LUMINOS Q.namix T; LUMINOS Q.namix R

LUMINOS Q.namix T; LUMINOS Q.namix R is an FDA 510(k)-cleared medical device (K250660) manufactured by Siemens Medical Solutions. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 13, 2025. Regulation: 8.