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Ge Lunar Corp.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K030962 DPX SERIES BRAVO DUO BONE DENSITOMETERKGI2003-07-25 View
510(k) K023554 DUAL-ENERGY VERTEBRAL ASSESSMENT VIEW SOFTWAREKGI2002-12-20 View
510(k) K011917 ADVANCED HIP ASSESSMENT SOFTWAREKGI2001-08-03 View
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