FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

Trex_HD

K Number: K162595 · Decision Nov 4, 2016
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
12
Review Days
50

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Basic Information

Device Name
Trex_HD
K Number
K162595
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)
Date Received
September 15, 2016
Decision Date
November 4, 2016
Product Code
GWQ
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
GWQ Full-Montage Standard Electroencephalograph

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Other Clearances by Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)

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K200878 Natus NeuroWorks
K173936 Natus Photic Stimulator
K180290 Natus Brain Monitor Amplifier
K180421 Natus NeuroWorks
K173690 Grass TWin
K172711 Comet-PLUS
K163163 XLTEK EMU40EX EEG Headbox
Search all 12 clearances from Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek) →