MODEL RM 6000, 6100,6200 POLYGRAPH

MODEL RM 6000, 6100,6200 POLYGRAPH is an FDA 510(k)-cleared medical device (K823281) manufactured by Nihon Kohden America, 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 December 21, 1982. Regulation: 8.