CVD PERIFLOW(TM) (SMALL VESSEL) BALLOON DILATATION CATHETER

CVD PERIFLOW(TM) (SMALL VESSEL) BALLOON DILATATION CATHETER is an FDA 510(k)-cleared medical device (K945693) manufactured by Cardiovascular Dynamics, 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 August 16, 1995. Regulation: 8.