FDA applicant

Anaerobe Systems

Mchenry, IL52 decisions1978–19850 recalls

FDA records 52 decisions for Anaerobe Systems (Mchenry, IL) from 1978 to 1985: 52 510(k) clearances. Most are in product codes JSI (Culture Media, Selective And Differential) and JTO (Discs, Strips And Reagents, Microorganism…). 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 Anaerobe Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anaerobe Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Anaerobe Systems

Which product codes does it file in?

What has FDA decided for it lately?