510(k) Report

FDA applicant

Liv Medica Products Pvt., Ltd.

Hockessin, DE1 decision2006–20060 recalls

FDA records 1 decision for Liv Medica Products Pvt., Ltd. (Hockessin, DE) in 2006: 1 510(k) clearance. All are in product code CBP (Valve, Non-Rebreathing). 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 Liv Medica Products Pvt., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Liv Medica Products Pvt., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Liv Medica Products Pvt., Ltd. 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?

  • CBPValve, Non-Rebreathing1decision

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.

  • K052458Liv Medica CPR Face MaskLiv Medica Products Pvt., Ltd. · 20061cites it

What has FDA decided for it lately?

  • K052458Liv Medica CPR Face MaskLiv Medica Products Pvt., Ltd. · 2006

The one decision as Liv Medica Products Pvt., Ltd. →