HRK-63-8 KNEE ARRAY COIL

HRK-63-8 KNEE ARRAY COIL is an FDA 510(k)-cleared medical device (K032633) 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 September 24, 2003. Regulation: 8.