510(k) Report

FDA applicant

Vas-Cath of Canada, Ltd.

Ontario, L5a 3v3, CA19 decisions1979–19881 recall

FDA records 19 decisions for Vas-Cath of Canada, Ltd. (Ontario, L5a 3v3, CA) from 1979 to 1988: 19 510(k) clearances. Most are in product codes LFJ (Catheter, Subclavian) and FIQ (Cannula, A-V Shunt). 1 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, gastroenterology and urology panel, where it files most

How often FDA has decided Vas-Cath of Canada, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vas-Cath of Canada, Ltd. since 2007.

Recalls per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

Class I Class II/III not classified

FIG. 1 — Vas-Cath of Canada, Ltd. 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?

  • LFJCatheter, Subclavian8decisions
  • FIQCannula, A-V Shunt3decisions
  • DQOCatheter, Intravascular, Diagnostic2decisions
  • BSOCatheter, Conduction, Anesthetic1decision
  • JCYCatheter, Infusion1decision
  • DQYCatheter, Percutaneous1decision

Also: CAZ (1), KNZ (1), FJS (1).

Who builds on its devices?

Later devices cite its devices 2 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.

  • K871488Vas-Cath Permanent Dual Lumen Hemodialysis CathVas-Cath of Canada, Ltd. · 19872cite it

What has FDA decided for it lately?

  • K875188Luer Lock Connectors / Ridig P.V.C.Vas-Cath of Canada, Ltd. · 1988
  • K871817Vas-Cath Peritoneal Dialysis CatheterVas-Cath of Canada, Ltd. · 1987
  • K871488Vas-Cath Permanent Dual Lumen Hemodialysis CathVas-Cath of Canada, Ltd. · 1987
  • K871487Vas-Cath Permanent Single Lumen Hemodialysis CathVas-Cath of Canada, Ltd. · 1987
  • K863982Vas-Cath Pericardiocentesis Catheter, Set & TrayVas-Cath of Canada, Ltd. · 1986
  • K853283Vaccess TM 4006Vas-Cath of Canada, Ltd. · 1985
  • K844854Opti-Flow Digital Subtraction Angiography Cat-KitVas-Cath of Canada, Ltd. · 1985
  • K844800Opti-Flow & Opti-Torque Angiographic CathetersVas-Cath of Canada, Ltd. · 1985

All 19 as Vas-Cath of Canada, Ltd. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K844433Guidewire, 70cm x 1mm, REF 5583705, Sterile, Single Use, BARD Access Systems…Aug 10, 2007