510(k) Report

FDA applicant

Viromed Laboratories, Inc.

Mchenry, IL25 decisions1983–19960 recalls

FDA records 25 decisions for Viromed Laboratories, Inc. (Mchenry, IL) from 1983 to 1996: 25 510(k) clearances. Most are in product codes KIR (Cells, Animal And Human, Cultured) and KIT (Media And Components, Synthetic Cell 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Viromed Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Viromed Laboratories, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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