PHILIPS SONO DIAGNOST 800

PHILIPS SONO DIAGNOST 800 is an FDA 510(k)-cleared medical device (K963706) manufactured by Hewlett-Packard Co.. 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 18, 1997. Regulation: 8.