FDA applicant

Nicolet Instrument Corp.

Madison, WI13 decisions1988–19930 recalls

FDA records 13 decisions for Nicolet Instrument Corp. (Madison, WI) from 1988 to 1993: 13 510(k) clearances. Most are in product codes IKN (Electromyograph, Diagnostic) and GWQ (Full-Montage Standard Electroencephalograph). 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 Nicolet Instrument Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nicolet Instrument Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Nicolet Instrument Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Nicolet”

FDA records each applicant name separately; these may or may not be the same firm.

Nicolet Biomedical Instruments 26 Nicolet Biomedical, Inc. 18

Nicolet Instrument Corp.

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?

Other applicant names beginning “Nicolet”