MAGNETIC RESONANCE DEVICE ACCESSORY SOFTWARE 4.0.

MAGNETIC RESONANCE DEVICE ACCESSORY SOFTWARE 4.0. is an FDA 510(k)-cleared medical device (K891541) manufactured by Diasonics, 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 May 10, 1989. Regulation: 8.