MAICO MB 11 WITH BERAPHONE PROBE

MAICO MB 11 WITH BERAPHONE PROBE is an FDA 510(k)-cleared medical device (K082035) manufactured by Maico Diagnostics. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 28, 2009. Regulation: 8.