FDA applicant

Tekpro

Mchenry, IL2 decisions1979–19790 recalls

FDA records 2 decisions for Tekpro (Mchenry, IL) in 1979: 2 510(k) clearances. Most are in product codes GKZ (Counter, Differential Cell) and KSY (Boxes, View, Blood Grouping). 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 Tekpro’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tekpro since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Tekpro

Which product codes does it file in?

What has FDA decided for it lately?