FDA applicant

Medipart Jerry Alexander

Cary, IL49 decisions1984–19900 recalls

FDA records 49 decisions for Medipart Jerry Alexander (Cary, IL) from 1984 to 1990: 49 510(k) clearances. Most are in product codes IYT (System, Rebreathing, Radionuclide) and CAH (Filter, Bacterial, Breathing-Circuit). 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 Medipart Jerry Alexander’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medipart Jerry Alexander since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medipart Jerry Alexander

Which product codes does it file in?

What has FDA decided for it lately?