510(k) Report

FDA applicant

Angiometrx, Inc.

Vancouver, Bc, CA3 decisions2003–20050 recalls

FDA records 3 decisions for Angiometrx, Inc. (Vancouver, Bc, CA) from 2003 to 2005: 3 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and LIT (Catheter, Angioplasty, Peripheral, Transluminal). 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 Angiometrx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Angiometrx, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Angiometrx, 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?

  • DQOCatheter, Intravascular, Diagnostic2decisions
  • LITCatheter, Angioplasty, Peripheral, Transluminal1decision

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.

  • K024000Metricath System Comprised of Metricath 1000 Console & Metricath Balloon CatheterAngiometrx, Inc. · 20031cites it
  • K042685Metricath SystemAngiometrx, Inc. · 20041cites it

What has FDA decided for it lately?

  • K051042Metricath Gemini-P Balloon Catheter, Models RX2515S-P, RX3015S-P, RX3515S-P, RX4015S-P, Metricath Console…Angiometrx, Inc. · 2005
  • K042685Metricath SystemAngiometrx, Inc. · 2004
  • K024000Metricath System Comprised of Metricath 1000 Console & Metricath Balloon CatheterAngiometrx, Inc. · 2003

All 3 as Angiometrx, Inc. →