DIASONICS SPA 3.5 MHZ, 30MM PROBE

DIASONICS SPA 3.5 MHZ, 30MM PROBE is an FDA 510(k)-cleared medical device (K864812) 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 March 9, 1987. Regulation: 8.