MindChild Medical, Inc. today announced that it has received clearance for its Pre-Marketing Notification (510(k)) from the US Food and Drug Administration (FDA) for its MERIDIAN non-invasive fetal heart monitor.
URL: http://www.news-medical.net/news/20120926/MindChild-receives-FDA-pre-market-clearance-for-MERIDIAN-non-invasive-fetal-heart-monitor.aspx
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