Get latest articles and stories on Business at LatestLY. New Delhi [India], July 26: In a major stride towards improving women's healthcare, Nesa Medtech, a prominent startup in women’s health, has announced that its groundbreaking Fibroid Mapping Reviewer Application (FMRA) has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). The FMRA technology represents a significant advancement that will aid physicians in planning minimally invasive image-guided treatments for uterine fibroids. Business News | Nesa Medtech Receives US FDA Clearance for Technology in Women’s Health.
Taiwan conducts military drill at Taoyuan Airport to prepare for possible Chinese invasion
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Nesa Medtech gets US FDA clearance for fibroid mapping reviewer application
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Nesa Medtech receives US FDA clearance for its fibroid mapping reviewer application
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