FDA applicant

Mogul Enterprises

San Jose, CA3 decisions2000–20030 recalls

FDA records 3 decisions for Mogul Enterprises (San Jose, CA) from 2000 to 2003: 3 510(k) clearances. All are in product code DRF (Catheter, Electrode Recording, Or Probe…). 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, cardiovascular panel, where it files most

How often FDA has decided Mogul Enterprises’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mogul Enterprises since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mogul Enterprises

Which product codes does it file in?

What has FDA decided for it lately?