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The Prometheus Group

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2016-04-15
TypeNumberDevice NameCodeDate
510(k) K160792 Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound IYO 2016-04-15 View