MAGNETIC RESONANCE DIAG DEVICE ACCESS APPLIC PKG

MAGNETIC RESONANCE DIAG DEVICE ACCESS APPLIC PKG is an FDA 510(k)-cleared medical device (K924426) 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 December 17, 1992. Regulation: 8.