510(k) Report

FDA applicant

Cardio Pulmonary Instruments

Mchenry, IL3 decisions1981–19810 recalls

FDA records 3 decisions for Cardio Pulmonary Instruments (Mchenry, IL) in 1981: 3 510(k) clearances. All are in product code BZC (Calculator, Pulmonary Function Data). 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 Cardio Pulmonary Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cardio Pulmonary Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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