510(k) Report

FDA applicant

Vsm Medtech, Ltd.

Vancouver, B.C., CA3 decisions2000–20030 recalls

FDA records 3 decisions for Vsm Medtech, Ltd. (Vancouver, B.C., CA) from 2000 to 2003: 3 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). Its devices cite 7 predicates, 2 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 Vsm Medtech, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vsm Medtech, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vsm Medtech, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vsm Medtech, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive3decisions

Whose devices does it build on?

Its devices cite 7 predicates; 2 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K994423Automated Non-Invasive Blood Pressure Monitor, Model BPM-100Vsm Medtech, Ltd. · 20002cite it

What has FDA decided for it lately?

  • K023078Bptru Vital Signs Monitor, Model BPM-300, & Bptru Portable Automated Non-Invasive Blood Pressure and…Vsm Medtech, Ltd. · 2003
  • K023055Bptru Portable Automated Non-Invasive Blood Pressure Monitor, Model BPM-200Vsm Medtech, Ltd. · 2002
  • K994423Automated Non-Invasive Blood Pressure Monitor, Model BPM-100Vsm Medtech, Ltd. · 2000

All 3 as Vsm Medtech, Ltd. →