QDR-1000 AND WITH X-RAY BONE DENSITOMETER

QDR-1000 AND WITH X-RAY BONE DENSITOMETER is an FDA 510(k)-cleared medical device (K905691) manufactured by Hologic, Inc.. 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 14, 1991. Regulation: 8.