# Devices For Vascular Intervention, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 14 (1987–1994): 14 510(k) clearances
- Product codes: LIT (5), DQY (2), MCW (2), DYB (2), DQO (1), DWF (1), MAV (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Fox Hollow Technologies: 4 (https://510kreport.com/company/fox-hollow-technologies)

## Its most-cited devices
- K883346: Simpson Peripheral Atherocath W/Addit. Size 13F (1988), cited by 1
- K881088: Addition of a Tip Guard to the Atherocath (TM) (1988), cited by 1
- K871011: Simpson Peripheral Atherocath (TM) (1987), cited by 1
- K874706: Modified Simpson Peripheral Atherocath (1988), cited by 1

## Recent decisions
- K935929: Microtrack (Mar 10, 1994)
- K920707: Hollow Motor Drive Unit W/ Torque Controller (Nov 23, 1992)
- K914422: Devices for Vascu Intervent Rotat Hemostat Valve (Dec 18, 1991)
- K911678: Rotating Hemostatic Valve (Jul 12, 1991)
- K910205: LP-60 Low Pressure Inflation Device (Feb 25, 1991)
- K901601: Hollow Motor Drive Unit (Jul 6, 1990)
- K883933: Introducing Catheter (Dec 2, 1988)
- K883981: Guiding Catheter (Tip Softness Change) (Nov 3, 1988)

Source page: https://510kreport.com/company/devices-for-vascular-intervention