FDA applicant
Manner Medical Products
FDA records 4 decisions for Manner Medical Products (Mchenry, IL) in 1976: 4 510(k) clearances. Most are in product codes CAT (Cannula, Nasal, Oxygen) and CBO (Attachment, Intermittent Mandatory Ventilation…). 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 Manner Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Manner Medical Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Manner Medical Products’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