LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6

LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6 is an FDA 510(k)-cleared medical device (K160277) manufactured by GE Medical Systems Ultrasound and Primary Care Diagnostics. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 24, 2016. Regulation: 8.