FDA applicant

Cdx Corp.

Mchenry, IL4 decisions1982–19850 recalls

FDA records 4 decisions for Cdx Corp. (Mchenry, IL) from 1982 to 1985: 4 510(k) clearances. Most are in product codes BZM (Calculator, Pulmonary Function Interpretor…) and BZG (Spirometer, Diagnostic). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Cdx Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Cdx Corp.

Which product codes does it file in?

What has FDA decided for it lately?