510(k) Report

FDA applicant

Medteq Innovations Pty, Ltd.

Rockville, MD1 decision2001–20010 recalls

FDA records 1 decision for Medteq Innovations Pty, Ltd. (Rockville, MD) in 2001: 1 510(k) clearance. All are in product code LIX (Aid, Cardiopulmonary Resuscitation). 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 Medteq Innovations Pty, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medteq Innovations Pty, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medteq Innovations Pty, Ltd.’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?

  • LIXAid, Cardiopulmonary Resuscitation1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K003937CPR Ezy Mask and PadMedteq Innovations Pty, Ltd. · 20011cites it

What has FDA decided for it lately?

  • K003937CPR Ezy Mask and PadMedteq Innovations Pty, Ltd. · 2001

The one decision as Medteq Innovations Pty, Ltd. →