GE HealthCare: new brain scanner approved by the FDA

(CercleFinance.com) - GE HealthCare announced Wednesday that the U.
S. Food and Drug Administration (FDA) has granted marketing approval for its latest brain magnetic resonance imaging (MRI) system.

The U.S.-based company says it has received 510(k) clearance from the FDA to market its high-performance Signa Magnus 3.0T device.

In a press release, GE HealthCare explains that its device offers new capabilities for clinical imaging and neuroscience, promoting the detection of neurological, oncological and psychiatric conditions.

From its point of view, this clearance highlights the progress it has made in the field of neuroimaging.

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