GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION

GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION is an FDA 510(k)-cleared medical device (K993364) 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 November 4, 1999. Regulation: 8.