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Invivo Corporation
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1.5T AND 3T 8-CHANNEL MEDIUM GENERAL PURPOSE FLEX COIL is an FDA 510(k)-cleared medical device (K111673) manufactured by Invivo Corporation. 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 22, 2011. Regulation: 8.