FDA applicant
Suzuken Co., Ltd.
FDA records 13 decisions for Suzuken Co., Ltd. (Mchenry, IL) from 1981 to 2018: 13 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and DSI (Detector And Alarm, Arrhythmia). Its devices cite 2 predicates, 1 of them its own earlier devices. 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 Suzuken Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2018
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Suzuken Co., 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