FDA applicant

Nordiclab Intl.

Mchenry, IL8 decisions1979–19800 recalls

FDA records 8 decisions for Nordiclab Intl. (Mchenry, IL) from 1979 to 1980: 8 510(k) clearances. Most are in product codes CHP (Radioimmunoassay, Estradiol) and CDZ (Radioimmunoassay, Testosterones And…). 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 Nordiclab Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nordiclab Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Nordiclab Intl.

Which product codes does it file in?

What has FDA decided for it lately?