FDA applicant

Boditestor

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Boditestor (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code CDM (Diazonium Colorimetry, Urobilinogen (Urinary…). 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 Boditestor’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Boditestor since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Boditestor

Which product codes does it file in?

What has FDA decided for it lately?