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Philips Receives FDA 510(k) Clearance for Lumify Ultrasound Device

Royal Philips today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for Lumify, its smart-device diagnostic ultrasound solution. The pocket-sized and lightweight S4-1 transducer now offers advanced sensitivity and exceptional high-resolution 2D image quality, along with new exam pre-sets, allowing clinicians to quickly triage and assess their patients like.
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