FDA 510(k) Applications Submitted by NIHON KOHDEN CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130238	01/31/2013	NIHON KOHDEN AE-918P NEURO UNIT	NIHON KOHDEN CORP.
K120397	02/08/2012	MEB-2300A NEUROPACK EVOKED POTENTIAL AND EMG MEASURING SYSTEM	NIHON KOHDEN CORP.
K110376	02/09/2011	PE-210AK SWITCH BOX	NIHON KOHDEN CORP.
K110410	02/14/2011	MS-120BK ELECTRIC STIMULATOR (EXTENSION UNIT)	NIHON KOHDEN CORP.
K110594	03/02/2011	GF-210R MULTI-GAS MODULE FOR NOHON KOHDEN BEDSIDE MONITORS	NIHON KOHDEN CORP.
K120888	03/23/2012	PSG-1100 SLEEP DIAGNOSTIC SYSTEM	NIHON KOHDEN CORP.
K122214	07/25/2012	TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)	NIHON KOHDEN CORP.
K102106	07/27/2010	NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION	NIHON KOHDEN CORP.
K102376	08/20/2010	NIHON KOHDEN CNS-6200 SERIES CENTRAL NURSE STATION, MODEL CNS-6201	NIHON KOHDEN CORP.