FDA applicant

Tracor Instruments, Inc.

Mchenry, IL10 decisions1976–19850 recalls

FDA records 10 decisions for Tracor Instruments, Inc. (Mchenry, IL) from 1976 to 1985: 10 510(k) clearances. Most are in product codes EWO (Audiometer) and GWF (Stimulator, Electrical, Evoked Response). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tracor Instruments, 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 Northern, Inc. 10 Tracor Instruments Austin, Inc. 1

Tracor Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Tracor”