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FDA 510(k)

MEDI-TRAC EEG ELECTRODE

K-Number: K950782 · 1995-06-22

Decision Date1995-06-22
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDI-TRAC EEG ELECTRODE 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 1995-06-22 under 510(k) number K950782. 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 MEDI-TRAC EEG ELECTRODE?

MEDI-TRAC EEG ELECTRODE is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Graphic Controls Corp.. The 510(k) number is K950782.

When did MEDI-TRAC EEG ELECTRODE receive FDA 510(k) clearance?

MEDI-TRAC EEG ELECTRODE received FDA 510(k) clearance on 1995-06-22, under 510(k) number K950782.

Who is the listed applicant for MEDI-TRAC EEG ELECTRODE?

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-TRAC EEG ELECTRODE?

The FDA product code for MEDI-TRAC EEG ELECTRODE is GXY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Graphic Controls Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 55 devices →

Related Devices (Code: GXY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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