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

Natus VikingQuest

K Number: K172743 · Decision Dec 19, 2017
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
74
Applicant Total
5
Review Days
98

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Basic Information

Device Name
Natus VikingQuest
K Number
K172743
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
890.1375
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Natus Neurology Incorporated
Date Received
September 12, 2017
Decision Date
December 19, 2017
Product Code
IKN
Advisory Committee
Physical Medicine
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
IKN Electromyograph, Diagnostic

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K Number Device Name
K243982 Nicolet EDX
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K173366 NicoletOne
K130346 SYNERGY FOCUS DESKTOP VERSION; SYNERGY FOCUS LAPTOP VERSION