# Vas-Cath, Inc.

- Location (FDA's records): Mississauga, Ontario, CA
- FDA decisions: 27 (1988–1998): 27 510(k) clearances
- Product codes: LIT (14), LFJ (5), FAD (2), LFK (2), FOZ (1), MPB (1), FKA (1), LJS (1)
- Predicates its devices cite: 6 (3 its own); citations of its devices by later devices: 11 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- Vas-Cath of Canada, Ltd.: 1 (https://510kreport.com/company/vas-cath-of-canada)

## Firms that cite its devices most
- C.R. Bard, Inc.: 5 (https://510kreport.com/company/cr-bard)
- Orbus Medical Technologies: 1 (https://510kreport.com/company/orbus-medical-technologies)
- Bolton Medical, Inc.: 1 (https://510kreport.com/company/bolton-medical)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)

## Its most-cited devices
- K965178: Niagara Dual Lumen Catheter (1997), cited by 3
- K933483: Opti-Plast 5F Pta Catheters (1993), cited by 2
- K973013: Opti-Plast (Centurion) 5.5F Angioplasty Catheter (1998), cited by 2
- K881743: Vas-Cath Flexxicon Dual Lumen Dialysis Catheter (1988), cited by 1
- K925485: Vas-Cath Inc. Opti-Plast Angioplasty Catheter (1994), cited by 1
- K914162: Vas-Cath Flexxicon 2 Dual Lumen Dialysis Catheters (1993), cited by 1

## Recent decisions
- K973013: Opti-Plast (Centurion) 5.5F Angioplasty Catheter (Jun 19, 1998)
- K965178: Niagara Dual Lumen Catheter (Aug 19, 1997)
- K964881: Ultraverse Pta Catheter (May 28, 1997)
- K970725: Opti-Plast XL 5.5 F Pta Catheter (May 9, 1997)
- K941706: Opti-Plast Angioplasty Catheter (Oct 18, 1994)
- K925485: Vas-Cath Inc. Opti-Plast Angioplasty Catheter (Mar 10, 1994)
- K933483: Opti-Plast 5F Pta Catheters (Sep 24, 1993)
- K914162: Vas-Cath Flexxicon 2 Dual Lumen Dialysis Catheters (Jul 1, 1993)

Source page: https://510kreport.com/company/vas-cath