Nihon Kohden Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151080Nihon Kohden CSM 1901 Bedside MonitorNovember 5, 2015
K130238NIHON KOHDEN AE-918P NEURO UNITMarch 4, 2015
K122214TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)May 21, 2013
K120888PSG-1100 SLEEP DIAGNOSTIC SYSTEMNovember 9, 2012
K120397MEB-2300A NEUROPACK EVOKED POTENTIAL AND EMG MEASURING SYSTEMSeptember 19, 2012
K112637NETKONNECT REMOTE NETWORK EXTENSIONDecember 9, 2011
K110594GF-210R MULTI-GAS MODULE FOR NOHON KOHDEN BEDSIDE MONITORSOctober 28, 2011
K110410MS-120BK ELECTRIC STIMULATOR (EXTENSION UNIT)August 4, 2011
K110376PE-210AK SWITCH BOXJuly 29, 2011
K102106NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATIONDecember 17, 2010
K102376NIHON KOHDEN CNS-6200 SERIES CENTRAL NURSE STATION, MODEL CNS-6201December 7, 2010