510(k) Report

FDA applicant

Healthcheck Corp.

Cheshire, CT9 decisions1984–19890 recalls

FDA records 9 decisions for Healthcheck Corp. (Cheshire, CT) from 1984 to 1989: 9 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). 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, cardiovascular panel, where it files most

How often FDA has decided Healthcheck Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Healthcheck Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Healthcheck Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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