HOLOGIC QDR-1000 X-RAY BONE DENSITOMETER/MODIFIED

HOLOGIC QDR-1000 X-RAY BONE DENSITOMETER/MODIFIED is an FDA 510(k)-cleared medical device (K883280) 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 September 28, 1988. Regulation: 8.