Cardiovascular Dynamics, Inc.
Cardiovascular Dynamics, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 1998.
Top product codes for Cardiovascular Dynamics, Inc.
Recent clearances by Cardiovascular Dynamics, Inc.
- K973713 — 22 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CATHETER/NEEDLE ASSEMBLY), 24 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CAR
- K971577 — FOCUS-PV BALLOON DILATATION CATHETER
- K963989 — P.D. ACCESS (PERCUTANEOUS DOPPLER) VASCULAR ACCESS DEVICE
- K963688 — FOCUS PV BALLOON DILATATION CATHETER
- K945693 — CVD PERIFLOW(TM) (SMALL VESSEL) BALLOON DILATATION CATHETER
- K952064 — FOCUS BALLOON DILATATION CATHETER
- K951502 — CVD BULLET INFUSION CATYHETER
- K951503 — CVD BULLETT HI-FLO INFUSION CATHETER
- K944016 — FOCUS BALLOON DILATATION CATHETER
- K945465 — CVD SMALL VESSEL BALLOON DILATATION CATHETER
- K943023 — CVD BULLETT PERIPHERAL INFUSION CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.