FDA applicant

E-Z Instruments Co.

San Antonio, TX1 decision1986–19860 recalls

FDA records 1 decision for E-Z Instruments Co. (San Antonio, TX) in 1986: 1 510(k) clearance. All are in product code GYA (Tester, Electrode/Lead, 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 E-Z Instruments Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E-Z Instruments Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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E-Z Instruments Co.

Which product codes does it file in?

What has FDA decided for it lately?