Nihon Kohden Corporation
Nihon Kohden Corporation holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2026.
Top product codes for Nihon Kohden Corporation
Recent clearances by Nihon Kohden Corporation
- K251641 — GF-310R Multigas Unit (GF-310R)
- K260747 — YP-710T Series NIBP Cuff; YP-840T Series Disposable Cuff
- K251366 — EEG-1260A Neurofax System (EEG-1260A); JE-940A EEG Amplifier Unit (JE-940A); LS-940A Photic Stimulator (LS-940A)
- K243956 — TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)
- K223567 — CNS-2101 Central Monitor
- K220976 — Life Scope PT BSM-1700 Series Bedside Monitor
- K213316 — Life Scope PT BSM-1700 Series, AY Series, Data Acquisition Unit, LIFE SCOPE BSM 6000 SERIES BEDSIDE MONITORING SYSTEM, Nihon Kohden CSM-1901 BEDSIDE MONITORING SYSTEM
- K203435 — Nihon Kohden Life Scope G5 Bedside Monitoring System, Nihon Kohden Life Scope G7 Bedside Monitoring System
- K201949 — Smart Cable NMT Module and Accessories, Life Scope BSM 3000 Series and Life Scope BSM 6000 Series
- K191975 — Elefix V Paste for EEG & EMG
- K190468 — Nihon Kohden SVM-7200 Series Vital Signs Monitor
- K183529 — AE-120A EEG Head Set
- K171765 — Nihon Kohden CO2 Monitor
- K171124 — Nihon Kohden Wireless Input Unit WEE-1200
- K163644 — Nihon Kohden QP-160AK EEG Trend Program
- K163459 — Nihon Kohden Vital Sign Telemeter
- K161860 — TG-970P CO2 Sensor Kit
- K153707 — Nihon Kohden Vital Sign Telemeter
- K152305 — Nihon Kohden Afib Detection Program QP-039P
- K142624 — Neuromaster G1 MEE200
Data sourced from openFDA. This site is unofficial and independent of the FDA.