KAVO ERGOCOM/ERGOCAM

KAVO ERGOCOM/ERGOCAM is an FDA 510(k)-cleared medical device (K050744) manufactured by Kavo America Corporation. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 20, 2005. Regulation: 8.