ECTON LYNX ULTRASOUND SYSTEM

ECTON LYNX ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K982800) manufactured by Ecton, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 21, 1998. Regulation: 8.