FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NIHON KOHDEN QP-160AK EEG TREND PROGRAM

K Number: K092573 · Decision Jul 9, 2010
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
15
Applicant Total
166
Review Days
323

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Basic Information

Device Name
NIHON KOHDEN QP-160AK EEG TREND PROGRAM
K Number
K092573
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nihon Kohden America, Inc.
Date Received
August 20, 2009
Decision Date
July 9, 2010
Product Code
OMA
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OMA Amplitude-Integrated Electroencephalograph

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OMA), ordered by most recent decision date.

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Other Clearances by Nihon Kohden America, Inc.

K Number Device Name
K113117 NIHON KOHDEN EEG-1200A WITH JE-120A MULTI CHANNEL ELECTRODE JUNCTION BOX
K120485 NIHON KOHDEN QP-160 AK TREND PROGRAM WITH THE ADDITION OF DSA ASYMMETRY TREND AND FFT P
K083456 NIHON KOHDEN CO2 SENSOR KIT, MODEL TG-970P
K083271 BSM-2300 &BSM6000 WITH CGS-9001 SERIES COMMUNICATION GATEWAY, MODEL CGS-9001 SERIES OPTIONAL ACCESSORY
K082785 NIHON KOHDEN BEDSIDE MONITOR, BSM 9100A SERIES
K071969 SEN-4100 ELECTRIC STIMULATOR
K080546 NIHON KOHDEN EEG-1200A SERIES NEUROFAX, MODEL EEG-1200A
K073550 PREFENSE EDNS-9000 SERIES NURSE CENTRAL STATION
K080342 NIHON KOHDEN BEDSIDE MONITOR, MODEL BSM-6000S SERIES
K073491 EEG-1100A SWITCH BOX
Search all 166 clearances from Nihon Kohden America, Inc. →