SCEPTOR SYSTEM AUTOMATED MODEL 216

SCEPTOR SYSTEM AUTOMATED MODEL 216 is an FDA 510(k)-cleared medical device (K810229) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 8, 1981. Regulation: 8.