FDA applicant
Amkor Trading Co.
FDA records 6 decisions for Amkor Trading Co. (Walker, MI) in 1984: 6 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMF (Syringe, Piston). 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 Amkor Trading Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Amkor Trading Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Amkor Trading Co.’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