PHILIPS IQON SPECTRAL CT

PHILIPS IQON SPECTRAL CT is an FDA 510(k)-cleared medical device (K133674) manufactured by Philips Healthcare (Cleveland). This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 2014. Regulation: 8.