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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