DIASONICS 3.5 GWA 30MM PROBE

DIASONICS 3.5 GWA 30MM PROBE is an FDA 510(k)-cleared medical device (K860361) 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 May 26, 1986. Regulation: 8.