KAC-300 KNEE ARRAY COIL

KAC-300 KNEE ARRAY COIL is an FDA 510(k)-cleared medical device (K993719) 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 November 25, 1999. Regulation: 8.