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Meridian Medical Systems, LLC
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UNIVERSAL DIGITAL INTERFACE (UDI) 1717 is an FDA 510(k)-cleared medical device (K103599) manufactured by Meridian Medical Systems, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 26, 2011. Regulation: 8.