
Esaote, S.p.A.
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MODIFICATION TO E-SCAN XQ is an FDA 510(k)-cleared medical device (K032121) manufactured by Esaote, S.p.A.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 12, 2003. Regulation: 8.