Nihon Kohden America, Inc. - FDA 510(k) Cleared Devices
166
Total
163
Cleared
0
Denied
48 devices
Cleared
Mar 22, 2012
NIHON KOHDEN EEG-1200A WITH JE-120A MULTI CHANNEL ELECTRODE JUNCTION BOX
Neurology
153d
Cleared
Mar 16, 2012
NIHON KOHDEN QP-160 AK TREND PROGRAM WITH THE ADDITION OF DSA ASYMMETRY TREND...
Neurology
28d
Cleared
Jul 09, 2010
NIHON KOHDEN QP-160AK EEG TREND PROGRAM
Neurology
323d
Cleared
Oct 06, 2008
SEN-4100 ELECTRIC STIMULATOR
Neurology
447d
Cleared
Aug 29, 2008
NIHON KOHDEN EEG-1200A SERIES NEUROFAX, MODEL EEG-1200A
Neurology
183d
Cleared
Jan 11, 2008
EEG-1100A SWITCH BOX
Neurology
30d
Cleared
Aug 17, 2005
MEE-1000A NEUROMASTER
Neurology
100d
Cleared
Apr 29, 2005
ELECTRODE JUNCTION BOX, MODEL JE-921A
Neurology
28d
Cleared
Jan 07, 2004
WIRELESS INPUT UNIT, MODEL WEE-1000A SERIES
Neurology
65d
Cleared
Jul 29, 2002
PSG INPUT BOX, MODEL JE-912AK
Neurology
28d
Cleared
Jun 28, 2001
NEUROPACK MICRO, MODEL MED-9100A SERIES
Neurology
121d
Cleared
May 08, 2001
NEUROFAX, MODELS EEG-1100A, EEG-9100A
Neurology
19d
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