510(k) Report

FDA applicant

Korr Medical Technologies, Inc.

Salt Lake City, UT2 decisions1998–20030 recalls

FDA records 2 decisions for Korr Medical Technologies, Inc. (Salt Lake City, UT) from 1998 to 2003: 2 510(k) clearances. Most are in product codes BZL (Computer, Oxygen-Uptake) and BZH (Meter, Peak Flow, Spirometry). Its devices cite 2 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, anesthesiology panel, where it files most

How often FDA has decided Korr Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Korr Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Korr 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?

  • BZLComputer, Oxygen-Uptake1decision
  • BZHMeter, Peak Flow, Spirometry1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K982995Accutrax, Model EPF840Korr Medical Technologies, Inc. · 19983cite it
  • K021490Reevue Indirect Calorimeter, Model#8100Korr Medical Technologies, Inc. · 20032cite it

What has FDA decided for it lately?

  • K021490Reevue Indirect Calorimeter, Model#8100Korr Medical Technologies, Inc. · 2003
  • K982995Accutrax, Model EPF840Korr Medical Technologies, Inc. · 1998

All 2 as Korr Medical Technologies, Inc. →