510(k) Report

FDA applicant

Jay-Mar INternational Enterprises, IN

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Jay-Mar INternational Enterprises, IN (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code ISB (Stimulator, Muscle, Diagnostic). 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, physical medicine panel, where it files most

How often FDA has decided Jay-Mar INternational Enterprises, IN’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jay-Mar INternational Enterprises, IN since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jay-Mar INternational Enterprises, IN by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • ISBStimulator, Muscle, Diagnostic1decision

What has FDA decided for it lately?

  • K780730FiguretrimJay-Mar INternational Enterprises, IN · 1978

The one decision as Jay-Mar INternational Enterprises, IN →