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Jan 10, 2005
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Iradimed gets FDA clearance for MRI infusion pump system
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IRadimed's MRidium 3870 IV Infusion Pump System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA).
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Lunit has updated its AI chest x-ray software, as well as secured the CE mark in Europe.
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The U.S. Food and Drug Administration (FDA) has cleared Hyperfine’s latest portable MRI software.
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