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Pulsonic Ag, Medical Technology
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CARDIOSCOPE SONOPLUS 3000 is an FDA 510(k)-cleared medical device (K051126) manufactured by Pulsonic Ag, Medical Technology. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 2005. Regulation: 8.