FDA applicant
Amdia Medical Products
FDA records 6 decisions for Amdia Medical Products (Mchenry, IL) in 1979: 6 510(k) clearances. Most are in product codes DQD (Stethoscope, Electronic) and GWZ (Percussor). 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 Amdia Medical Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Amdia Medical Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Amdia 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