Nihon Kohden Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nihon Kohden Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Nihon Kohden Corp. has 9 FDA 510(k) cleared medical devices. Based in Foothill, US.
Historical record: 9 cleared submissions from 2010 to 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Nihon Kohden Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nihon Kohden Corp.
9 devices
Cleared
Mar 04, 2015
NIHON KOHDEN AE-918P NEURO UNIT
Neurology
762d
Cleared
May 21, 2013
TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)
Anesthesiology
300d
Cleared
Nov 09, 2012
PSG-1100 SLEEP DIAGNOSTIC SYSTEM
Neurology
231d
Cleared
Sep 19, 2012
MEB-2300A NEUROPACK EVOKED POTENTIAL AND EMG MEASURING SYSTEM
Neurology
224d
Cleared
Oct 28, 2011
GF-210R MULTI-GAS MODULE FOR NOHON KOHDEN BEDSIDE MONITORS
Anesthesiology
240d
Cleared
Aug 04, 2011
MS-120BK ELECTRIC STIMULATOR (EXTENSION UNIT)
Neurology
171d
Cleared
Jul 29, 2011
PE-210AK SWITCH BOX
Neurology
170d
Cleared
Dec 17, 2010
NIHON KHDEN PREFENSE EDNS-9000 SERIES CENTRAL NURSE STATION
Cardiovascular
143d
Cleared
Dec 07, 2010
NIHON KOHDEN CNS-6200 SERIES CENTRAL NURSE STATION, MODEL CNS-6201
Cardiovascular
109d