FLEXART QD HEAD/NECK COIL

FLEXART QD HEAD/NECK COIL is an FDA 510(k)-cleared medical device (K961391) manufactured by Toshiba America Mri, 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 July 8, 1996. Regulation: 8.