FDA applicant

Immulok, Inc.

Mchenry, IL15 decisions1981–19830 recalls

FDA records 15 decisions for Immulok, Inc. (Mchenry, IL) from 1981 to 1983: 15 510(k) clearances. Most are in product codes GQL (Antisera, Fluorescent, Herpesvirus Hominis 1,2) and DHN (Antinuclear Antibody, Indirect…). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Immulok, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Immulok, Inc.

Which product codes does it file in?

What has FDA decided for it lately?