DILON 6800 ACELLA (ACELLA)

DILON 6800 ACELLA (ACELLA) is an FDA 510(k)-cleared medical device (K110384) manufactured by Dilon Technologies, Inc.. This device is classified under the Radiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 2, 2011. Regulation: 8.