SuperSonic Imagine has announces it has received 510(k) clearance from the FDA and authorisation to use the CE marking from the LNE/GMed for its new cutting-edge smart ultrasound system, the Aixplorer MACH 30. “The FDA 510(k) and CE Mark are critical milestones in the launch of our exciting new system,” explained Michèle Lesieur, SuperSonic Imagine CEO and Chairwoman of its Board of Directors.
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