Nihon Kohden Corporation
FDA 510(k) medical device clearances.
Top product codes for Nihon Kohden Corporation
Recent clearances by Nihon Kohden Corporation
- 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.