CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRE

CARDIOMETRICS FLOWIRE DOPPLER GUIDE WIRE is an FDA 510(k)-cleared medical device (K943022) manufactured by Cardio Metrics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 18, 1994. Regulation: 8.