Very preterm infants are at high risk for adverse neurodevelopmental outcomes. Magnetic resonance imaging (MRI) has been proposed as a means of predicting neurodevelopmental outcomes in this ...

Today, the U.S. Food and Drug Administration cleared the first magnetic resonance imaging (MRI) device specifically for neonatal brain and head imaging in neonatal intensive care units (NICU).

The erroneous view that neonatal brain injury is uniform and due primarily to acquired insults such as birth asphyxia is slowly being modified by epidemiologic studies. 5 The causes of neonatal brain ...

The U.S. Food and Drug Administration yesterday approved the first magnetic resonance imaging (MRI) device that can be specifically used in neonates or newborn babies. These MRI devices would be used ...

(WASHINGTON) — The U.S. Food and Drug Administration on Thursday approved the first MRI device specifically for neonatal brain and head imaging in neonatal intensive care units. “Although we can use ...

Eyas Medical Imaging, Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Ascent3T™ Neonatal Magnetic Resonance Imaging (MRI) System, a whole-body magnetic resonance ...

Aspect Imaging is happy to announce that the U.S. Food and Drugs Administration has granted its Embrace Neonatal magnetic resonance imaging device clearance for commercial and medical use inside ...

Growing emphasis on neonatal brain injury assessment, transport-risk reduction in intensive care units, and expanding NICU infrastructure are driving global demand for specialized neonatal MRI systems ...

“510(k) clearance marks a significant milestone for the company and reflects our mission to enable healthcare professionals to save more babies’ lives with state-of-the-art, precision imaging,” said ...