BRAVO MULTI-MODALITY SYSTEM

BRAVO MULTI-MODALITY SYSTEM is an FDA 510(k)-cleared medical device (K991054) manufactured by Nicolet Biomedical, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 2, 1999. Regulation: 8.