
General Electric Co.
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GE VOLUSON 730 PRO/EXPERT BT03 ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K032620) 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 October 9, 2003. Regulation: 8.