LOGIQ P10, LOGIQ P9, LOGIQ P8

LOGIQ P10, LOGIQ P9, LOGIQ P8 is an FDA 510(k)-cleared medical device (K214039) 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 21, 2022. Regulation: 8.