FDA applicant

American Convertors Div., American Pharmaseal

Mchenry, IL19 decisions1980–19840 recalls

FDA records 19 decisions for American Convertors Div., American Pharmaseal (Mchenry, IL) from 1980 to 1984: 19 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and FRG (Wrap, Sterilization). 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 and plastic surgery panel, where it files most

How often FDA has decided American Convertors Div., American Pharmaseal’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Convertors Div., American Pharmaseal since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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American Convertors Div., American Pharmaseal

Which product codes does it file in?

What has FDA decided for it lately?