
Ge Lunar Corp.
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DPX SERIES BRAVO DUO BONE DENSITOMETER is an FDA 510(k)-cleared medical device (K030962) manufactured by Ge Lunar Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 24, 2003. Regulation: 8.