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FDA 510(k)

EEG ELECTRODE PAD

K-Number: K841877 · 1984-07-19

ApplicantNeurologics, Inc.
Decision Date1984-07-19
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EEG ELECTRODE PAD is the device name listed in this FDA 510(k) record. The listed applicant is Neurologics, Inc.. It received FDA 510(k) clearance on 1984-07-19 under 510(k) number K841877. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EEG ELECTRODE PAD?

EEG ELECTRODE PAD is a medical device that received FDA 510(k) clearance on 1984-07-19. The listed applicant is Neurologics, Inc.. The 510(k) number is K841877.

When did EEG ELECTRODE PAD receive FDA 510(k) clearance?

EEG ELECTRODE PAD received FDA 510(k) clearance on 1984-07-19, under 510(k) number K841877.

Who is the listed applicant for EEG ELECTRODE PAD?

The FDA 510(k) record lists Neurologics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EEG ELECTRODE PAD?

The FDA product code for EEG ELECTRODE PAD is GXY.

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Related Devices (Code: GXY)

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Official Source

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