# Vas-Cath of Canada, Ltd.

- Location (FDA's records): Ontario, L5a 3v3, CA
- FDA decisions: 19 (1979–1988): 19 510(k) clearances
- Product codes: LFJ (8), FIQ (3), DQO (2), BSO (1), JCY (1), DQY (1), CAZ (1), KNZ (1), FJS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Vas-Cath, Inc.: 1 (https://510kreport.com/company/vas-cath)

## Its most-cited devices
- K871488: Vas-Cath Permanent Dual Lumen Hemodialysis Cath (1987), cited by 2

## Recent decisions
- K875188: Luer Lock Connectors / Ridig P.V.C. (Mar 2, 1988)
- K871817: Vas-Cath Peritoneal Dialysis Catheter (Jul 16, 1987)
- K871488: Vas-Cath Permanent Dual Lumen Hemodialysis Cath (Jun 12, 1987)
- K871487: Vas-Cath Permanent Single Lumen Hemodialysis Cath (Jun 12, 1987)
- K863982: Vas-Cath Pericardiocentesis Catheter, Set & Tray (Oct 24, 1986)
- K853283: Vaccess TM 4006 (Aug 22, 1985)
- K844854: Opti-Flow Digital Subtraction  Angiography Cat-Kit (May 21, 1985)
- K844800: Opti-Flow & Opti-Torque Angiographic Catheters (May 16, 1985)

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