510(k) Report

FDA applicant

Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits

Hamburg, DE2 decisions2002–20020 recalls

FDA records 2 decisions for Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits (Hamburg, DE) in 2002: 2 510(k) clearances. All are in product code BZD (Ventilator, Non-Continuous (Respirator)). Its devices cite 4 predicates, 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 Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits 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?

  • BZDVentilator, Non-Continuous (Respirator)2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K013738Weinmann SomnomaskGottlieb Weinmann Geraete Fuer Medizin Und Arbeits · 20021cites it

What has FDA decided for it lately?

  • K022934Silentflow 2 Exhalation System, Model WM 23650Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits · 2002
  • K013738Weinmann SomnomaskGottlieb Weinmann Geraete Fuer Medizin Und Arbeits · 2002

All 2 as Gottlieb Weinmann Geraete Fuer Medizin Und Arbeits →