510(k) Report

FDA applicant

Noninvasive Medical Technology Corp.

Ogden, UT2 decisions1992–19930 recalls

FDA records 2 decisions for Noninvasive Medical Technology Corp. (Ogden, UT) from 1992 to 1993: 2 510(k) clearances. Most are in product codes DQA (Oximeter) and JPI (Device, Hematocrit Measuring). 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 Noninvasive Medical Technology Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Noninvasive Medical Technology Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Noninvasive Medical Technology 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?

  • DQAOximeter1decision
  • JPIDevice, Hematocrit Measuring1decision

Who builds on its devices?

Later devices cite its devices 3 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.

  • K910077Crit-ScanNoninvasive Medical Technology Corp. · 19922cite it
  • K924167Crit-LineNoninvasive Medical Technology Corp. · 19931cites it

What has FDA decided for it lately?

  • K924167Crit-LineNoninvasive Medical Technology Corp. · 1993
  • K910077Crit-ScanNoninvasive Medical Technology Corp. · 1992

All 2 as Noninvasive Medical Technology Corp. →

Other applicant names beginning “Noninvasive”

FDA records each applicant name separately; these may or may not be the same firm.

Noninvasive Medical Technologies, Inc. 4