Nihon Kohden America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nihon Kohden America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NIHON KOHDEN EEG-1200A WITH JE-120A MULTI CHANNEL ELECTRODE JUNCTION BOX, NIHON KOHDEN QP-160 AK TREND PROGRAM WITH THE ADDITION OF DSA ASYMMETRY TREND AND FFT P, NIHON KOHDEN QP-160AK EEG TREND PROGRAM
166
Total
163
Cleared
0
Denied
Nihon Kohden America, Inc. has 163 FDA 510(k) cleared medical devices. Based in Foothill Ranch, US.
Historical record: 163 cleared submissions from 1979 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nihon Kohden America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nihon Kohden America, Inc.
166 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
Mar 02, 2009
NIHON KOHDEN CO2 SENSOR KIT, MODEL TG-970P
Anesthesiology
101d
Cleared
Dec 24, 2008
BSM-2300 &BSM6000 WITH CGS-9001 SERIES COMMUNICATION GATEWAY, MODEL CGS-9001...
Cardiovascular
48d
Cleared
Nov 26, 2008
NIHON KOHDEN BEDSIDE MONITOR, BSM 9100A SERIES
Cardiovascular
64d
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
Mar 28, 2008
PREFENSE EDNS-9000 SERIES NURSE CENTRAL STATION
Cardiovascular
101d
Cleared
Feb 26, 2008
NIHON KOHDEN BEDSIDE MONITOR, MODEL BSM-6000S SERIES
Cardiovascular
18d
Cleared
Jan 11, 2008
EEG-1100A SWITCH BOX
Neurology
30d
Cleared
Nov 29, 2007
YG-125T AND YG-135T NASAL ADAPTER
Anesthesiology
56d
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