LOGIQ S7 EXPERT, LOGIQ S7 PRO

LOGIQ S7 EXPERT, LOGIQ S7 PRO is an FDA 510(k)-cleared medical device (K122114) 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 October 2, 2012. Regulation: 8.