Medical Device Manufacturer · US , Irvine , CA

Cardiovascular Dynamics, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1994

Total

Cleared

Denied

Cardiovascular Dynamics, Inc. has 11 FDA 510(k) cleared cardiovascular devices. Based in Irvine, US.

Historical record: 11 cleared submissions from 1994 to 1998.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cardiovascular Dynamics, Inc.

11 devices

1-11 of 11

Cleared Jan 23, 1998

22 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CATHETER/NEEDLE ASSEMBLY), 24...

K973713 · ITX

Radiology · 116d

Cleared Jun 18, 1997

FOCUS-PV BALLOON DILATATION CATHETER

K971577 · LIT

Cardiovascular · 58d

Cleared Apr 24, 1997

P.D. ACCESS (PERCUTANEOUS DOPPLER) VASCULAR ACCESS DEVICE

K963989 · ITX

Radiology · 202d

Cleared Mar 28, 1997

FOCUS PV BALLOON DILATATION CATHETER

K963688 · LIT

Cardiovascular · 193d

Cleared Aug 17, 1995

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

K945693 · LIT

Cardiovascular · 269d

Cleared Jun 21, 1995

FOCUS BALLOON DILATATION CATHETER

K952064 · LIT

Cardiovascular · 50d

Cleared May 10, 1995

CVD BULLET INFUSION CATYHETER

K951502 · KRA

Cardiovascular · 43d

Cleared May 04, 1995

CVD BULLETT HI-FLO INFUSION CATHETER

K951503 · KRA

Cardiovascular · 37d

Cleared Dec 20, 1994

FOCUS BALLOON DILATATION CATHETER

K944016 · LIT

Cardiovascular · 126d

Cleared Dec 20, 1994

CVD SMALL VESSEL BALLOON DILATATION CATHETER

K945465 · LIT

Cardiovascular · 43d

Cleared Sep 30, 1994

CVD BULLETT PERIPHERAL INFUSION CATHETER

K943023 · FOZ

General Hospital · 98d

Cardiovascular Dynamics, Inc. - FDA 510(k) Cleared Devices

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