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Siemens Medi Cal Solutions, Inc.
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13C/1H OCCIPITAL HEADCOIL FOR MAGNETOM ALLEGRA is an FDA 510(k)-cleared medical device (K042718) manufactured by Siemens Medi Cal Solutions, 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 November 11, 2004. Regulation: 8.