SONOS 500 AND SONOS 1000 ULTRASOUND IMAGING SYSTEM

SONOS 500 AND SONOS 1000 ULTRASOUND IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K905728) manufactured by Hewlett-Packard Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 1991. Regulation: 8.