Hologic, Inc.
1.10-YEAR FRACTURE RISK QUESTIONNAIRE OPTION FOR QDR X-RAY BONE DENSITOMETER, MODEL QDR OPTION
SKU K080711UPC KGI
In Stock
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IIFDA 510(k) Cleared (K080711)
1
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Hologic, Inc.
Free shipping on orders over $99 · 30-day returns
1.10-YEAR FRACTURE RISK QUESTIONNAIRE OPTION FOR QDR X-RAY BONE DENSITOMETER, MODEL QDR OPTION is an FDA 510(k)-cleared medical device (K080711) 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 1, 2008. Regulation: 8.
