FDA Grants 510(k) Clearance For Philips’ SmartSpeed Precise - Data Intelligence

FDA Grants 510(k) Clearance For Philips’ SmartSpeed Precise - Data Intelligence

The software delivers a brain scan in under ten seconds. Credit: © Koninklijke Philips N.V. The US Food and Drug Administration (FDA) has granted 510(k) clearance for Philips’ SmartSpeed Precise deep learning reconstruction software. This dual AI software is said to deliver up to three times faster scanning and 80% sharper images, bolstering diagnostic confidence in cardiology, oncology, and neurology. Approved for clinical use, SmartSpeed Preci…

FDA grants 510(k) clearance for Philips’ deep learning reconstruction software

The US Food and Drug Administration (FDA) has granted 510(k) clearance for Philips’ SmartSpeed Precise deep learning reconstruction software.The post FDA grants 510(k) clearance for Philips’ deep learning reconstruction software appeared first on Medical Device Network.

FDA Clears SmartSpeed Precise MRI Software from Philips

The deep learning reconstruction software reportedly facilitates accelerated MRI scanning and significantly enhanced image sharpness.