SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS

SONOS 500, 1000, 1500/SONOS OR ULTRASOUND IMAG SYS is an FDA 510(k)-cleared medical device (K921863) manufactured by Hewlett-Packard Co.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 27, 1992. Regulation: 8.