Nihon Kohden Corporation - FDA 510(k) Cleared Devices
Recent clearances: YP-710T Series NIBP Cuff, EEG-1260A Neurofax System (EEG-1260A), TG-980P CO2 Sensor Kit (TG-980P)
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nihon Kohden Corporation Anesthesiology ✕
6 devices
Cleared
Jun 10, 2025
TG-980P CO2 Sensor Kit (TG-980P)
Anesthesiology
169d
Cleared
Jul 21, 2022
Life Scope PT BSM-1700 Series Bedside Monitor
Anesthesiology
108d
Cleared
Dec 29, 2021
Life Scope PT BSM-1700 Series, AY Series, Data Acquisition Unit, LIFE SCOPE...
Anesthesiology
86d
Cleared
May 02, 2021
Smart Cable NMT Module and Accessories, Life Scope BSM 3000 Series and Life...
Anesthesiology
293d
Cleared
Oct 11, 2017
Nihon Kohden CO2 Monitor
Anesthesiology
119d
Cleared
Feb 24, 2017
TG-970P CO2 Sensor Kit
Anesthesiology
233d