FDA applicant

Lee Medical Intl., Inc.

Mchenry, IL8 decisions1983–19840 recalls

FDA records 8 decisions for Lee Medical Intl., Inc. (Mchenry, IL) from 1983 to 1984: 8 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMF (Syringe, Piston). 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, general hospital panel, where it files most

How often FDA has decided Lee Medical Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lee Medical Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lee Medical Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?