VECTRA PRO MODELS 2 AND 4

VECTRA PRO MODELS 2 AND 4 is an FDA 510(k)-cleared medical device (K982324) manufactured by Chattanooga Group, 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 January 31, 1999. Regulation: 8.