HOLOGIC QDR-1000/W X-RAY BONE DENSITOMETER

HOLOGIC QDR-1000/W X-RAY BONE DENSITOMETER is an FDA 510(k)-cleared medical device (K894795) 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 August 29, 1990. Regulation: 8.