
Konica Minolta Medical & Graphic, Inc.
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KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM is an FDA 510(k)-cleared medical device (K110717) manufactured by Konica Minolta Medical & Graphic, 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 December 22, 2011. Regulation: 8.