DIASONICS ITNRAOPERATIVE PROBES

DIASONICS ITNRAOPERATIVE PROBES is an FDA 510(k)-cleared medical device (K961002) manufactured by Diasonics Ultrasound. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 21, 1997. Regulation: 8.