PHILIPS CT DYNAMIC MYOCARDIAL PERFUSION (DMP) APPLICATION

PHILIPS CT DYNAMIC MYOCARDIAL PERFUSION (DMP) APPLICATION is an FDA 510(k)-cleared medical device (K133603) manufactured by Philips Medical Systems. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 24, 2014. Regulation: 8.