FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER

FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER is an FDA 510(k)-cleared medical device (K983269) 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 November 17, 1998. Regulation: 8.