Devices For Vascular Intervention, Inc.
FDA 510(k) medical device clearances.
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.