510(k) Report

FDA applicant

Canamet Canadian Natl Medical Technologies, Inc.

Deer Field, IL1 decision2004–20040 recalls

FDA records 1 decision for Canamet Canadian Natl Medical Technologies, Inc. (Deer Field, IL) in 2004: 1 510(k) clearance. All are in product code DXN (System, Measurement, Blood-Pressure…). Its devices cite 5 predicates, 0 of them its own earlier devices. 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 Canamet Canadian Natl Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Canamet Canadian Natl Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Canamet Canadian Natl Medical Technologies, 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?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive1decision

Whose devices does it build on?

Its devices cite 5 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K041169Piesometer, Model MK-1Canamet Canadian Natl Medical Technologies, Inc. · 2004

The one decision as Canamet Canadian Natl Medical Technologies, Inc. →