DIASONICS QT ENDORECTAL 7.5 MHZ PROBE

DIASONICS QT ENDORECTAL 7.5 MHZ PROBE is an FDA 510(k)-cleared medical device (K880714) manufactured by Diasonics, 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 April 20, 1988. Regulation: 8.