Devices For Vascular Intervention, Inc.
Devices For Vascular Intervention, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 1994.
Top product codes for Devices For Vascular Intervention, Inc.
Recent clearances by Devices For Vascular Intervention, Inc.
- K935929 — MICROTRACK
- K920707 — HOLLOW MOTOR DRIVE UNIT W/ TORQUE CONTROLLER
- K914422 — DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE
- K911678 — ROTATING HEMOSTATIC VALVE
- K910205 — LP-60 LOW PRESSURE INFLATION DEVICE
- K901601 — HOLLOW MOTOR DRIVE UNIT
- K883933 — INTRODUCING CATHETER
- K883981 — GUIDING CATHETER (TIP SOFTNESS CHANGE)
- K883916 — ROTATING HEMOSTATIC VALVE
- K883346 — SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F
- K881088 — ADDITION OF A TIP GUARD TO THE ATHEROCATH(TM)
- K874706 — MODIFIED SIMPSON PERIPHERAL ATHEROCATH
- K871021 — GUIDING CATHETERS 9F JL4
- K871011 — SIMPSON PERIPHERAL ATHEROCATH(TM)
Data sourced from openFDA. This site is unofficial and independent of the FDA.