GE VIVID 3 EXPERT; GE VIVID 3 PRO

GE VIVID 3 EXPERT; GE VIVID 3 PRO is an FDA 510(k)-cleared medical device (K020789) manufactured by General Electric Co.. 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 3, 2002. Regulation: 8.