FDA Clears Emagine’s Mobile Ultrasound Device

February 27, 2020

The FDA granted Emagine Solutions 510(k) clearance for its VistaScan mobile ultrasound system.

The platform allows clinicians to use smart phones or tablets to conduct handheld ultrasounds on the go, using FDA cleared ultrasound probes that work with the system’s mobile app.

The system also allows for high-precision manipulation of the ultrasound image using the smartphone or tablet’s touchscreen.

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