FDA applicant
Cairco, Ltd.
FDA records 9 decisions for Cairco, Ltd. (Mchenry, IL) from 1981 to 1982: 9 510(k) clearances. Most are in product codes CBK (Ventilator, Continuous, Facility Use) and BZK (Spirometer, Monitoring (W/Wo Alarm)). 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 Cairco, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cairco, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cairco, Ltd.’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