SERVO MED NYSTAGMOGRAPH NG-1

SERVO MED NYSTAGMOGRAPH NG-1 is an FDA 510(k)-cleared medical device (K843004) manufactured by Servo Med, 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 October 29, 1984. Regulation: 8.