510(k) Report

FDA applicant

Cheshire Diagnostics, Ltd.

Cheshire, GB6 decisions2002–20020 recalls

FDA records 6 decisions for Cheshire Diagnostics, Ltd. (Cheshire, GB) in 2002: 6 510(k) clearances. Most are in product codes MSV (System,Test,Antibodies,B2 - Glycoprotein I (B2…) and MID (System, Test, Anticardiolipin Immunological). 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, immunology panel, where it files most

How often FDA has decided Cheshire Diagnostics, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cheshire Diagnostics, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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