REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER

REFERENCE POPULATION FOR NORLAND APOLLO X-RAY BONE DENSITOMETER is an FDA 510(k)-cleared medical device (K980125) manufactured by Norland 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 May 19, 1998. Regulation: 8.