
Fujifilm Medical Systems U.S.A, Inc.
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SYNAPSE 3D NODULE ANALYSIS is an FDA 510(k)-cleared medical device (K120679) manufactured by Fujifilm Medical Systems U.S.A, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 2012. Regulation: 8.