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FDA 510(k)

EEG GEL

K-Number: K781493 · 1979-04-17

ApplicantGraphic Controls Corp.
Decision Date1979-04-17
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EEG GEL is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1979-04-17 under 510(k) number K781493. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EEG GEL?

EEG GEL is a medical device that received FDA 510(k) clearance on 1979-04-17. The listed applicant is Graphic Controls Corp.. The 510(k) number is K781493.

When did EEG GEL receive FDA 510(k) clearance?

EEG GEL received FDA 510(k) clearance on 1979-04-17, under 510(k) number K781493.

Who is the listed applicant for EEG GEL?

The FDA 510(k) record lists Graphic Controls Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EEG GEL?

The FDA product code for EEG GEL is GYB.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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