FDA applicant

Precision Cap Systems

Mchenry, IL7 decisions1983–19830 recalls

FDA records 7 decisions for Precision Cap Systems (Mchenry, IL) in 1983: 7 510(k) clearances. All are in product code GXY (Electrode, Cutaneous). 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 Precision Cap Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Precision Cap Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Precision Cap Systems

Which product codes does it file in?

What has FDA decided for it lately?