HOLOGIC QDR SERIES X-RAY BOE DENSITOMETERS

HOLOGIC QDR SERIES X-RAY BOE DENSITOMETERS is an FDA 510(k)-cleared medical device (K963363) 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 November 21, 1996. Regulation: 8.