FDA applicant

Tracor Northern, Inc.

Middleton, WI10 decisions1981–19880 recalls

FDA records 10 decisions for Tracor Northern, Inc. (Middleton, WI) from 1981 to 1988: 10 510(k) clearances. Most are in product codes GWF (Stimulator, Electrical, Evoked Response) and OLT (Non-Normalizing Quantitative…). 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 Tracor Northern, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tracor Northern, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Tracor”

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

Tracor Instruments, Inc. 10 Tracor Instruments Austin, Inc. 1

Tracor Northern, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Tracor”