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Medison Co., Ltd.
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SONOVIEW PRO BY MEDISON CO., LTD. is an FDA 510(k)-cleared medical device (K031886) manufactured by Medison Co., Ltd.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 29, 2003. Regulation: 8.