NEUROAMP EEG AMPLIFIER— 510(k) K974495

Substantially Equivalent

Neurocorp, Ltd.

FDA 510(k) clearance K974495 for NEUROAMP EEG AMPLIFIER, Substantially Equivalent on 1998-02-26. Applicant: Neurocorp, Ltd.. Device class: 2.

Clearance details

Applicant: Neurocorp, Ltd.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1997-11-28
Decision date: 1998-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tarrytown, NY, US

Download summary PDF View on FDA.gov ↗

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