FOREARM SOFTWARE FOR LUNAR DPX SERIES BONE DESITOM

FOREARM SOFTWARE FOR LUNAR DPX SERIES BONE DESITOM is an FDA 510(k)-cleared medical device (K915535) manufactured by Lunar. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 26, 1992. Regulation: 8.