Fujifilm ECHELON Synergy MRI System Gains FDA 510(k) Clearance

FDA clears Fujifilm’s ECHELON Synergy MRI system via 510(k). The device is classified as a nuclear magnetic resonance imaging system (product code LNH).

• Cleared through the FDA 510(k) pathway.
• Product code LNH designates a nuclear magnetic resonance imaging system.
• Manufactured by Fujifilm Corporation.

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