510(k) Report

FDA applicant

Oxytec Medical Corporation

Mccordsville, IN1 decision2005–20050 recalls

FDA records 1 decision for Oxytec Medical Corporation (Mccordsville, IN) in 2005: 1 510(k) clearance. All are in product code CAW (Generator, Oxygen, Portable). Its devices cite 1 predicate, 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 Oxytec Medical Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oxytec Medical Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Oxytec Medical Corporation 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?

  • CAWGenerator, Oxygen, Portable1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

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.

  • K043615Oxytec, Model 900Oxytec Medical Corporation · 20052cite it

What has FDA decided for it lately?

  • K043615Oxytec, Model 900Oxytec Medical Corporation · 2005

The one decision as Oxytec Medical Corporation →