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FDA 510(k)

MEDI-TRACE EEG CREME

K-Number: K790818 · 1979-06-05

ApplicantGraphic Controls Corp.
Decision Date1979-06-05
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDI-TRACE EEG CREME 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 1979-06-05 under 510(k) number K790818. 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 MEDI-TRACE EEG CREME?

MEDI-TRACE EEG CREME is a medical device that received FDA 510(k) clearance on 1979-06-05. The listed applicant is Graphic Controls Corp.. The 510(k) number is K790818.

When did MEDI-TRACE EEG CREME receive FDA 510(k) clearance?

MEDI-TRACE EEG CREME received FDA 510(k) clearance on 1979-06-05, under 510(k) number K790818.

Who is the listed applicant for MEDI-TRACE EEG CREME?

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 MEDI-TRACE EEG CREME?

The FDA product code for MEDI-TRACE EEG CREME is GYB.

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Other records listing Graphic Controls Corp. as applicant

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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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