510(k) Report

FDA applicant

Dynotec Corp.

San Diego, CA1 decision1994–19940 recalls

FDA records 1 decision for Dynotec Corp. (San Diego, CA) in 1994: 1 510(k) clearance. All are in product code CAW (Generator, Oxygen, Portable). 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 Dynotec Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynotec Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • CAWGenerator, Oxygen, Portable1decision

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.

  • K942082Model 6323 Oxygen ConcentratorDynotec Corp. · 19942cite it

What has FDA decided for it lately?

  • K942082Model 6323 Oxygen ConcentratorDynotec Corp. · 1994

The one decision as Dynotec Corp. →