FDA applicant
Cardio Pulmonary Instruments
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
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.
Planning a device like Cardio Pulmonary Instruments’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