510(k) Report

FDA applicant

Devices For Vascular Intervention, Inc.

Redwood City, CA14 decisions1987–19940 recalls

FDA records 14 decisions for Devices For Vascular Intervention, Inc. (Redwood City, CA) from 1987 to 1994: 14 510(k) clearances. Most are in product codes LIT (Catheter, Angioplasty, Peripheral, Transluminal) and DQY (Catheter, Percutaneous). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Devices For Vascular Intervention, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Devices For Vascular Intervention, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Devices For Vascular Intervention, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LITCatheter, Angioplasty, Peripheral, Transluminal5decisions
  • DQYCatheter, Percutaneous2decisions
  • MCWCatheter, Peripheral, Atherectomy2decisions
  • DYBIntroducer, Catheter2decisions
  • DQOCatheter, Intravascular, Diagnostic1decision
  • DWFCatheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass1decision

Also: MAV (1).

Who builds on its devices?

Later devices cite its devices 4 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K883346Simpson Peripheral Atherocath W/Addit. Size 13FDevices For Vascular Intervention, Inc. · 19881cites it
  • K881088Addition of a Tip Guard to the Atherocath (TM)Devices For Vascular Intervention, Inc. · 19881cites it
  • K871011Simpson Peripheral Atherocath (TM)Devices For Vascular Intervention, Inc. · 19871cites it
  • K874706Modified Simpson Peripheral AtherocathDevices For Vascular Intervention, Inc. · 19881cites it

What has FDA decided for it lately?

  • K935929MicrotrackDevices For Vascular Intervention, Inc. · 1994
  • K920707Hollow Motor Drive Unit W/ Torque ControllerDevices For Vascular Intervention, Inc. · 1992
  • K914422Devices for Vascu Intervent Rotat Hemostat ValveDevices For Vascular Intervention, Inc. · 1991
  • K911678Rotating Hemostatic ValveDevices For Vascular Intervention, Inc. · 1991
  • K910205LP-60 Low Pressure Inflation DeviceDevices For Vascular Intervention, Inc. · 1991
  • K901601Hollow Motor Drive UnitDevices For Vascular Intervention, Inc. · 1990
  • K883933Introducing CatheterDevices For Vascular Intervention, Inc. · 1988
  • K883981Guiding Catheter (Tip Softness Change)Devices For Vascular Intervention, Inc. · 1988

All 14 as Devices For Vascular Intervention, Inc. →