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Mri Devices Corp.
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KFA-12 KNEE, FOOT, AND ANKLE ARRAY COIL is an FDA 510(k)-cleared medical device (K033151) manufactured by Mri Devices Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 2003. Regulation: 8.