510(k) Report

FDA applicant

Medtrac Technologies Corp.

Lakewood, CO1 decision1994–19940 recalls

FDA records 1 decision for Medtrac Technologies Corp. (Lakewood, CO) in 1994: 1 510(k) clearance. All are in product code BZH (Meter, Peak Flow, Spirometry). 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, anesthesiology panel, where it files most

How often FDA has decided Medtrac Technologies Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtrac Technologies Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medtrac Technologies Corp. 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?

  • BZHMeter, Peak Flow, Spirometry1decision

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.

  • K940835Peaklog and Display SoftwareMedtrac Technologies Corp. · 19942cite it

What has FDA decided for it lately?

  • K940835Peaklog and Display SoftwareMedtrac Technologies Corp. · 1994

The one decision as Medtrac Technologies Corp. →