Devices For Vascular Intervention, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Devices For Vascular Intervention, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Devices For Vascular Intervention, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Redwood City, US.
Historical record: 14 cleared submissions from 1987 to 1994.
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 - Devices For Vascular Intervention, Inc.
14 devices
Cleared
Mar 10, 1994
MICROTRACK
Cardiovascular
87d
Cleared
Nov 23, 1992
HOLLOW MOTOR DRIVE UNIT W/ TORQUE CONTROLLER
Cardiovascular
279d
Cleared
Dec 18, 1991
DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE
Cardiovascular
76d
Cleared
Jul 12, 1991
ROTATING HEMOSTATIC VALVE
Cardiovascular
88d
Cleared
Feb 25, 1991
LP-60 LOW PRESSURE INFLATION DEVICE
Cardiovascular
40d
Cleared
Jul 06, 1990
HOLLOW MOTOR DRIVE UNIT
Cardiovascular
91d
Cleared
Dec 02, 1988
INTRODUCING CATHETER
Cardiovascular
78d
Cleared
Nov 03, 1988
GUIDING CATHETER (TIP SOFTNESS CHANGE)
Cardiovascular
43d
Cleared
Oct 28, 1988
ROTATING HEMOSTATIC VALVE
Cardiovascular
42d
Cleared
Sep 26, 1988
SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F
Cardiovascular
60d
Cleared
May 31, 1988
ADDITION OF A TIP GUARD TO THE ATHEROCATH(TM)
Cardiovascular
77d
Cleared
Jan 04, 1988
MODIFIED SIMPSON PERIPHERAL ATHEROCATH
Cardiovascular
61d
Cleared
Jun 16, 1987
GUIDING CATHETERS 9F JL4
Cardiovascular
92d
Cleared
May 14, 1987
SIMPSON PERIPHERAL ATHEROCATH(TM)
Cardiovascular
62d