WISCONSIN DUAL-PHOTON BONE ANALYZER

WISCONSIN DUAL-PHOTON BONE ANALYZER is an FDA 510(k)-cleared medical device (K802180) manufactured by Lunar Radiation 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 December 30, 1980. Regulation: 8.