Suzuken Co., Ltd.
Suzuken Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2018.
Top product codes for Suzuken Co., Ltd.
Recent clearances by Suzuken Co., Ltd.
- K172068 — Kenz Cardico1211
- K101024 — KENZ CARDY302 MAX
- K092389 — DISPOSAL ECG ELECTRODES, MODEL EASYRODE
- K001896 — KENZ ECG 108 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS; KENZ ECG 110 SINGLE CHANNEL DIGITAL ELECTROCARDIOGRAPHS WITH EC
- K870443 — KENZ-CARDICO 1201
- K862544 — KENZ-ECG-102 SINGLE CHANNEL ELECTROCARDIOGRAPH
- K843731 — KENZ 80Z MARK II
- K822968 — ELECTROCARDIOGRAPH INTERPRETER
- K820854 — KENZ-45M
- K820991 — KENZ-GELECT GEL PAD
- K812263 — KENZ-GELECT
- K811949 — KENL-ECG-3
- K811950 — KENL-ECG
Data sourced from openFDA. This site is unofficial and independent of the FDA.