MODIFIED RADIUS - MODEL NUMBER MM 5000

MODIFIED RADIUS - MODEL NUMBER MM 5000 is an FDA 510(k)-cleared medical device (K871727) manufactured by Ultrasonix, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 29, 1987. Regulation: 8.