SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI

SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI is an FDA 510(k)-cleared medical device (K900472) manufactured by Skytron, Div. the Kmw Group, Inc.. This device is classified under the Neurology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 3, 1990. Regulation: 8.