FDA applicant

Parasitic Disease Consultants

Mchenry, IL3 decisions1983–19830 recalls

FDA records 3 decisions for Parasitic Disease Consultants (Mchenry, IL) in 1983: 3 510(k) clearances. Most are in product codes GLZ (Antigens, If, Toxoplasma Gondii) and JWL (Antigen, Treponema Pallidum For Fta-Abs Test). 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 Parasitic Disease Consultants’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Parasitic Disease Consultants since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Parasitic Disease Consultants

Which product codes does it file in?

What has FDA decided for it lately?