
Eemagine Medical Imaging Solutions GmbH
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MAXINSIGHT is an FDA 510(k)-cleared medical device (K070358) manufactured by Eemagine Medical Imaging Solutions GmbH. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 29, 2007. Regulation: 8.