EarliTec Diagnostics Receives FDA 510(k) Authorization for Next-Generation EarliPoint Evaluation for Autism Spectrum Disorder

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EarliTec Diagnostics, Inc. (“EarliTec”), a digital health company developing novel diagnostic and therapeutic products for children with autism spectrum disorder (ASD) and early childhood vulnerabilities, today announced U.S. Food and Drug Administration (FDA) 510(k) authorization of the second generation of its EarliPoint™ Evaluation for ASD for children ages 16-30 months old.