510(k) Report

FDA applicant

Vsm Technology, Inc.

Washington, DC2 decisions2000–20010 recalls

FDA records 2 decisions for Vsm Technology, Inc. (Washington, DC) from 2000 to 2001: 2 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). 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 Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vsm Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vsm Technology, 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-Invasive2decisions

Who builds on its devices?

Later devices cite its devices 5 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.

  • K012636Bptru Automated Non-Invasive Blood Pressure Monitor, Model BPM-100Vsm Technology, Inc. · 20013cite it
  • K002046Modification to Automated Non-Invasive Blood Pressure Monitor, Model BPM-100Vsm Technology, Inc. · 20002cite it

What has FDA decided for it lately?

  • K012636Bptru Automated Non-Invasive Blood Pressure Monitor, Model BPM-100Vsm Technology, Inc. · 2001
  • K002046Modification to Automated Non-Invasive Blood Pressure Monitor, Model BPM-100Vsm Technology, Inc. · 2000

All 2 as Vsm Technology, Inc. →