FDA applicant

Electrical Geodesics, Incorporated

Eugene, OR7 decisions2001–20141 recall

FDA records 7 decisions for Electrical Geodesics, Incorporated (Eugene, OR) from 2001 to 2014: 7 510(k) clearances. Most are in product codes GWQ (Full-Montage Standard Electroencephalograph) and OLT (Non-Normalizing Quantitative…). Its devices cite 8 predicates, 4 of them its own earlier devices. 1 recall is linked to its devices, 1 Class I.

FDA’s records also spell it “Electrical Geodesics, Inc.”.

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 Electrical Geodesics, Incorporated’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2021

2007high 1 (2021) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Electrical Geodesics, Incorporated’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 “Electrical”

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

Electrical Systems Div. 1

Electrical Geodesics, Incorporated

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Electrical”