
Hitachi Medical Systems America, Inc.
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MAGNETIC RESONANCE DIAGNOSTIC DEVICE is an FDA 510(k)-cleared medical device (K072279) manufactured by Hitachi Medical Systems America, 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 September 20, 2007. Regulation: 8.