EXPANDED REFERENCE VALUES FOR DPX BON DENSITOMETERS

EXPANDED REFERENCE VALUES FOR DPX BON DENSITOMETERS is an FDA 510(k)-cleared medical device (K964307) manufactured by 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 April 15, 1997. Regulation: 8.