FDA applicant
Canadian Monaghan, Ltd.
FDA records 5 decisions for Canadian Monaghan, Ltd. (London, Ontario, CA) from 1987 to 1993: 5 510(k) clearances. All are in product code CAP (Monitor, Airway Pressure (Includes Gauge…). 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 Canadian Monaghan, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Canadian Monaghan, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Canadian Monaghan, 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