FDA applicant

Marathon

Mchenry, IL3 decisions1982–19820 recalls

FDA records 3 decisions for Marathon (Mchenry, IL) in 1982: 3 510(k) clearances. Most are in product codes CAW (Generator, Oxygen, Portable) and CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Marathon since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Marathon”

FDA records each applicant name separately; these may or may not be the same firm.

Marathon Management Co. 1

Marathon

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Marathon”