510(k) Report

FDA applicant

Buchler Instruments, Inc.

Mchenry, IL2 decisions1976–19790 recalls

FDA records 2 decisions for Buchler Instruments, Inc. (Mchenry, IL) from 1976 to 1979: 2 510(k) clearances. Most are in product codes KHO (Fluorometer, For Clinical Use) and JIT (Calibrator, Secondary). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Buchler Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Buchler Instruments, Inc. 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?

  • KHOFluorometer, For Clinical Use1decision
  • JITCalibrator, Secondary1decision

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.

  • K791312Catalog #4-2520 Chloridometer ChlorideBuchler Instruments, Inc. · 19791cites it

What has FDA decided for it lately?

  • K791312Catalog #4-2520 Chloridometer ChlorideBuchler Instruments, Inc. · 1979
  • K760506Hemaflour ZPBuchler Instruments, Inc. · 1976

All 2 as Buchler Instruments, Inc. →