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Analogic Corp.
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SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250 is an FDA 510(k)-cleared medical device (K043025) manufactured by Analogic Corp.. 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 18, 2004. Regulation: 8.