FDA 510(k), K101386, VIGILANT EEG MONITOR MODEL VIGILANT 2.0

FDA 510(k), K101386, VIGILANT EEG MONITOR MODEL VIGILANT 2.0

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510(K) Number: K101386
Device Name: VIGILANT EEG MONITOR MODEL VIGILANT 2.0
Manufacturer:
Device Classification Name: Full-Montage Standard Electroencephalograph
Regulation Number: 882.1400
Classification Product Code: GWQ
Date Received: 05/18/2010
Decision Date: 07/30/2010
Regulation Medical Specialty: Neurology
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