Nihon Kohden Corporation - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
FDA 510(k) cleared devices by Nihon Kohden Corporation Cardiovascular ✕
6 devices
Cleared
Jul 31, 2023
CNS-2101 Central Monitor
Cardiovascular
244d
Cleared
Jul 16, 2021
Nihon Kohden Life Scope G5 Bedside Monitoring System, Nihon Kohden Life Scope...
Cardiovascular
235d
Cleared
May 28, 2019
Nihon Kohden SVM-7200 Series Vital Signs Monitor
Cardiovascular
91d
Cleared
Apr 04, 2017
Nihon Kohden Vital Sign Telemeter
Cardiovascular
116d
Cleared
Sep 02, 2016
Nihon Kohden Vital Sign Telemeter
Cardiovascular
254d
Cleared
Apr 08, 2016
Nihon Kohden Afib Detection Program QP-039P
Cardiovascular
238d