IRREGULAR CURVE TRACING REVISITION & DOPPLER

IRREGULAR CURVE TRACING REVISITION & DOPPLER is an FDA 510(k)-cleared medical device (K853769) 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 October 30, 1985. Regulation: 8.