FDA applicant

Supelco, Inc.

Mchenry, IL24 decisions1976–19890 recalls

FDA records 24 decisions for Supelco, Inc. (Mchenry, IL) from 1976 to 1989: 24 510(k) clearances. Most are in product codes DPM (Columns, Liquid Chromatography) and DKB (Calibrators, Drug Mixture). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Supelco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Supelco, Inc.

Which product codes does it file in?

What has FDA decided for it lately?