Cardio-Dynamics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardio-Dynamics, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cardio-Dynamics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 4 cleared submissions from 1994 to 1995. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardio-Dynamics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardio-Dynamics, Inc.
4 devices
Cleared
Dec 01, 1995
FOCUS PC BALLOON DILATATION CATHETER
Cardiovascular
77d
Cleared
Feb 24, 1995
CVD PERIFLOW(TM) BALLOON DILATATION CATHETER
Cardiovascular
81d
Cleared
Aug 02, 1994
CVD SMALL VESSEL BALLOON DILATION CATHETER
Cardiovascular
91d
Cleared
Feb 04, 1994
BULLETT PERIPHERAL INFUSION CATHETER
General Hospital
340d