DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER

DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER is an FDA 510(k)-cleared medical device (K861023) manufactured by Diagnostic Electronics Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 16, 1986. Regulation: 8.