FDA applicant

Farrall Instruments, Inc.

Mchenry, IL7 decisions1976–19950 recalls

FDA records 7 decisions for Farrall Instruments, Inc. (Mchenry, IL) from 1976 to 1995: 7 510(k) clearances. Most are in product codes LIL (Monitor, Penile Tumescence) and HCB (Device, Aversive Conditioning). 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, neurology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Farrall Instruments, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Farrall Instruments, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?