
Monica Veytia
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KANTERON DICOM STATION (KDS), MODEL 3.0 is an FDA 510(k)-cleared medical device (K073176) manufactured by Monica Veytia. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2008. Regulation: 8.