PULSED DOPPLER OPTION, CONTINU-WAVE

PULSED DOPPLER OPTION, CONTINU-WAVE is an FDA 510(k)-cleared medical device (K842407) manufactured by General Electric 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 February 12, 1985. Regulation: 8.