SkyLife receives FDA clearance

October 30, 2017

NeoLight announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Skylife™ portable phototherapy system. The Skylife device delivers a narrow band of high-intensity blue light via blue light emitting diodes (LEDs) to provide treatment for neonatal unconjugated hyperbilirubinemia (jaundice).

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