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

NIHON KOHDEN AE-918P NEURO UNIT

K Number: K130238 · Decision Mar 4, 2015
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
15
Applicant Total
9
Review Days
762

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Basic Information

Device Name
NIHON KOHDEN AE-918P NEURO UNIT
K Number
K130238
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 Corp.
Date Received
January 31, 2013
Decision Date
March 4, 2015
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

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