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The Newman Group, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K090465 DIGDOP ULTRASOUND SYSTEMITX2009-04-08 View
510(k) K061091 BABYBEAT CORDLESSKNG2006-05-04 View
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