ENDOSONICS AUTOMATIC PULL BACK DEVICE

ENDOSONICS AUTOMATIC PULL BACK DEVICE is an FDA 510(k)-cleared medical device (K962293) manufactured by Endosonics Corp.. 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 15, 1996. Regulation: 8.