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FDA 510(k) Applications Submitted by Natus Neurology Incorporated
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130346
02/11/2013
SYNERGY FOCUS DESKTOP VERSION; SYNERGY FOCUS LAPTOP VERSION
NATUS NEUROLOGY INCORPORATED
K172743
09/12/2017
Natus VikingQuest
Natus Neurology Incorporated
K173366
10/26/2017
NicoletOne
Natus Neurology Incorporated
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