
Siemens Medical Solutions USA, Inc.
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ARTISTE SOLUTION WITH SYS_VB50 UPDATE is an FDA 510(k)-cleared medical device (K103606) manufactured by Siemens Medical Solutions USA, 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 April 14, 2011. Regulation: 8.