GE LOGIQ 9 MODEL 2375600

GE LOGIQ 9 MODEL 2375600 is an FDA 510(k)-cleared medical device (K030934) manufactured by Ge Medical Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 16, 2003. Regulation: 8.