510(k) Report

FDA applicant

Ibp Instruments GmbH

Hannover, DE3 decisions2002–20030 recalls

FDA records 3 decisions for Ibp Instruments GmbH (Hannover, DE) from 2002 to 2003: 3 510(k) clearances. Most are in product codes FIZ (Meter, Conductivity, Non-Remote) and FKH (Solution-Test Standard-Conductivity, Dialysis). Its devices cite 3 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, gastroenterology and urology panel, where it files most

How often FDA has decided Ibp Instruments GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ibp Instruments GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ibp Instruments GmbH 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?

  • FIZMeter, Conductivity, Non-Remote2decisions
  • FKHSolution-Test Standard-Conductivity, Dialysis1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 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.

  • K020908HDM97Ibp Instruments GmbH · 20022cite it
  • K032075Conductivity Standard Solution-MetercareIbp Instruments GmbH · 20031cites it
  • K020909HDM99Ibp Instruments GmbH · 20021cites it

What has FDA decided for it lately?

  • K032075Conductivity Standard Solution-MetercareIbp Instruments GmbH · 2003
  • K020908HDM97Ibp Instruments GmbH · 2002
  • K020909HDM99Ibp Instruments GmbH · 2002

All 3 as Ibp Instruments GmbH →