LOGIQ P9 and LOGIQ P7

LOGIQ P9 and LOGIQ P7 is an FDA 510(k)-cleared medical device (K163596) manufactured by GE Healthcare. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 9, 2017. Regulation: 8.