# Suzuken Co., Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 13 (1981–2018): 13 510(k) clearances
- Product codes: DPS (5), DSI (2), GYB (2), DRX (1), LOS (1), DXN (1), MWJ (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ge Medical Systems Information Technologies: 1 (https://510kreport.com/company/ge-medical-systems-information-technologies)

## Its most-cited devices
- K870443: Kenz-Cardico 1201 (1987), cited by 1

## Recent decisions
- K172068: Kenz Cardico1211 (Jun 1, 2018)
- K101024: Kenz CARDY302 Max (Jan 6, 2011)
- K092389: Disposal Ecg Electrodes, Model Easyrode (Oct 13, 2009)
- K001896: Kenz Ecg 108 Single Channel Digital Electrocardiographs; Kenz Ecg 110 Single Channel Digital Electrocardiographs with EC (Jan 8, 2001)
- K870443: Kenz-Cardico 1201 (Jul 1, 1987)
- K862544: Kenz-Ecg-102 Single Channel Electrocardiograph (Aug 6, 1986)
- K843731: Kenz 80Z Mark II (Jul 11, 1985)
- K822968: Electrocardiograph Interpreter (Dec 15, 1982)

Source page: https://510kreport.com/company/suzuken